Name: rs35450965
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs35450965

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:9474824-9474847 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / d…
del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₀ / dup(T)₁₁ / ins(T)₃₀ / ins(T)₃₁ / ins(T)₃₂ / ins(T)₃₅ / ins(T)₃₆ / ins(T)₅₁
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1764 (1224/6937, ALFA)
(T)₂₄=0.0067 (26/3854, ALSPAC)
(T)₂₄=0.0038 (14/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF560 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6937	TTTTTTTTTTTTTTTTTTTTTTTT=0.7423	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0170, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1764, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0213, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0137, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0293, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.772727	0.109364	0.117908	32
European	Sub	5869	TTTTTTTTTTTTTTTTTTTTTTTT=0.6962	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0199, TTTTTTTTTTTTTTTTTTTTTTTTT=0.2080, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0252, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0162, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0344, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.723058	0.13325	0.143693	32
African	Sub	702	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	20	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	682	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	32	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	198	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	98	TTTTTTTTTTTTTTTTTTTTTTTT=0.95	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.957447	0.021277	0.021277	11

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6937	(T)₂₄=0.7423	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0170, dupT=0.1764, dupTT=0.0213, dupTTT=0.0293, dup(T)₄=0.0137, dup(T)₇=0.0000
Allele Frequency Aggregator	European	Sub	5869	(T)₂₄=0.6962	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0199, dupT=0.2080, dupTT=0.0252, dupTTT=0.0344, dup(T)₄=0.0162, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	702	(T)₂₄=1.000	del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	198	(T)₂₄=1.000	del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	98	(T)₂₄=0.95	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.01, dupT=0.03, dupTT=0.00, dupTTT=0.01, dup(T)₄=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	32	(T)₂₄=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	22	(T)₂₄=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(T)₂₄=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₇=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.9933
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.9962

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 19	NC_000019.10:g.9474836_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474837_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474838_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474839_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474840_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474841_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474842_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474843_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474844_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474845_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474846_9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474847del
GRCh38.p14 chr 19	NC_000019.10:g.9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474846_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474845_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474844_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474843_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474842_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474841_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474840_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474838_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474837_9474847dup
GRCh38.p14 chr 19	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 19	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585512_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585513_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585514_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585515_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585516_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585517_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585518_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585519_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585520_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585521_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585522_9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585523del
GRCh37.p13 chr 19	NC_000019.9:g.9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585522_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585521_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585520_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585519_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585518_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585517_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585516_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585514_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585513_9585523dup
GRCh37.p13 chr 19	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ZNF560 RefSeqGene	NG_054924.1:g.36858_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36859_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36860_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36861_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36862_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36863_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36864_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36865_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36866_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36867_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36868_36869del
ZNF560 RefSeqGene	NG_054924.1:g.36869del
ZNF560 RefSeqGene	NG_054924.1:g.36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36868_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36867_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36866_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36865_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36864_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36863_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36862_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36860_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36859_36869dup
ZNF560 RefSeqGene	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 RefSeqGene	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 RefSeqGene	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 RefSeqGene	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 RefSeqGene	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 RefSeqGene	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: ZNF560, zinc finger protein 560 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF560 transcript variant 2	NM_001351678.2:c.-285+449… NM_001351678.2:c.-285+449_-285+460del	N/A	Intron Variant
ZNF560 transcript variant 1	NM_152476.3:c.30+449_30+4… NM_152476.3:c.30+449_30+460del	N/A	Intron Variant
ZNF560 transcript variant X3	XM_011527696.3:c.30+449_3… XM_011527696.3:c.30+449_30+460del	N/A	Intron Variant
ZNF560 transcript variant X2	XM_011527697.3:c.30+449_3… XM_011527697.3:c.30+449_30+460del	N/A	Intron Variant
ZNF560 transcript variant X1	XR_007066601.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₄=	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₀	dup(T)₁₁	ins(T)₃₀	ins(T)₃₁	ins(T)₃₂	ins(T)₃₅	ins(T)₃₆	ins(T)₅₁
GRCh38.p14 chr 19	NC_000019.10:g.9474824_9474847=	NC_000019.10:g.9474836_9474847del	NC_000019.10:g.9474837_9474847del	NC_000019.10:g.9474838_9474847del	NC_000019.10:g.9474839_9474847del	NC_000019.10:g.9474840_9474847del	NC_000019.10:g.9474841_9474847del	NC_000019.10:g.9474842_9474847del	NC_000019.10:g.9474843_9474847del	NC_000019.10:g.9474844_9474847del	NC_000019.10:g.9474845_9474847del	NC_000019.10:g.9474846_9474847del	NC_000019.10:g.9474847del	NC_000019.10:g.9474847dup	NC_000019.10:g.9474846_9474847dup	NC_000019.10:g.9474845_9474847dup	NC_000019.10:g.9474844_9474847dup	NC_000019.10:g.9474843_9474847dup	NC_000019.10:g.9474842_9474847dup	NC_000019.10:g.9474841_9474847dup	NC_000019.10:g.9474840_9474847dup	NC_000019.10:g.9474838_9474847dup	NC_000019.10:g.9474837_9474847dup	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:g.9474847_9474848insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.9585500_9585523=	NC_000019.9:g.9585512_9585523del	NC_000019.9:g.9585513_9585523del	NC_000019.9:g.9585514_9585523del	NC_000019.9:g.9585515_9585523del	NC_000019.9:g.9585516_9585523del	NC_000019.9:g.9585517_9585523del	NC_000019.9:g.9585518_9585523del	NC_000019.9:g.9585519_9585523del	NC_000019.9:g.9585520_9585523del	NC_000019.9:g.9585521_9585523del	NC_000019.9:g.9585522_9585523del	NC_000019.9:g.9585523del	NC_000019.9:g.9585523dup	NC_000019.9:g.9585522_9585523dup	NC_000019.9:g.9585521_9585523dup	NC_000019.9:g.9585520_9585523dup	NC_000019.9:g.9585519_9585523dup	NC_000019.9:g.9585518_9585523dup	NC_000019.9:g.9585517_9585523dup	NC_000019.9:g.9585516_9585523dup	NC_000019.9:g.9585514_9585523dup	NC_000019.9:g.9585513_9585523dup	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.9:g.9585523_9585524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ZNF560 RefSeqGene	NG_054924.1:g.36846_36869=	NG_054924.1:g.36858_36869del	NG_054924.1:g.36859_36869del	NG_054924.1:g.36860_36869del	NG_054924.1:g.36861_36869del	NG_054924.1:g.36862_36869del	NG_054924.1:g.36863_36869del	NG_054924.1:g.36864_36869del	NG_054924.1:g.36865_36869del	NG_054924.1:g.36866_36869del	NG_054924.1:g.36867_36869del	NG_054924.1:g.36868_36869del	NG_054924.1:g.36869del	NG_054924.1:g.36869dup	NG_054924.1:g.36868_36869dup	NG_054924.1:g.36867_36869dup	NG_054924.1:g.36866_36869dup	NG_054924.1:g.36865_36869dup	NG_054924.1:g.36864_36869dup	NG_054924.1:g.36863_36869dup	NG_054924.1:g.36862_36869dup	NG_054924.1:g.36860_36869dup	NG_054924.1:g.36859_36869dup	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_054924.1:g.36869_36870insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 transcript variant 2	NM_001351678.2:c.-285+460=	NM_001351678.2:c.-285+449_-285+460del	NM_001351678.2:c.-285+450_-285+460del	NM_001351678.2:c.-285+451_-285+460del	NM_001351678.2:c.-285+452_-285+460del	NM_001351678.2:c.-285+453_-285+460del	NM_001351678.2:c.-285+454_-285+460del	NM_001351678.2:c.-285+455_-285+460del	NM_001351678.2:c.-285+456_-285+460del	NM_001351678.2:c.-285+457_-285+460del	NM_001351678.2:c.-285+458_-285+460del	NM_001351678.2:c.-285+459_-285+460del	NM_001351678.2:c.-285+460del	NM_001351678.2:c.-285+460dup	NM_001351678.2:c.-285+459_-285+460dup	NM_001351678.2:c.-285+458_-285+460dup	NM_001351678.2:c.-285+457_-285+460dup	NM_001351678.2:c.-285+456_-285+460dup	NM_001351678.2:c.-285+455_-285+460dup	NM_001351678.2:c.-285+454_-285+460dup	NM_001351678.2:c.-285+453_-285+460dup	NM_001351678.2:c.-285+451_-285+460dup	NM_001351678.2:c.-285+450_-285+460dup	NM_001351678.2:c.-285+460_-285+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001351678.2:c.-285+460_-285+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001351678.2:c.-285+460_-285+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001351678.2:c.-285+460_-285+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001351678.2:c.-285+460_-285+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001351678.2:c.-285+460_-285+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 transcript variant 1	NM_152476.2:c.30+460=	NM_152476.2:c.30+449_30+460del	NM_152476.2:c.30+450_30+460del	NM_152476.2:c.30+451_30+460del	NM_152476.2:c.30+452_30+460del	NM_152476.2:c.30+453_30+460del	NM_152476.2:c.30+454_30+460del	NM_152476.2:c.30+455_30+460del	NM_152476.2:c.30+456_30+460del	NM_152476.2:c.30+457_30+460del	NM_152476.2:c.30+458_30+460del	NM_152476.2:c.30+459_30+460del	NM_152476.2:c.30+460del	NM_152476.2:c.30+460dup	NM_152476.2:c.30+459_30+460dup	NM_152476.2:c.30+458_30+460dup	NM_152476.2:c.30+457_30+460dup	NM_152476.2:c.30+456_30+460dup	NM_152476.2:c.30+455_30+460dup	NM_152476.2:c.30+454_30+460dup	NM_152476.2:c.30+453_30+460dup	NM_152476.2:c.30+451_30+460dup	NM_152476.2:c.30+450_30+460dup	NM_152476.2:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.2:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.2:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.2:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.2:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.2:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 transcript variant 1	NM_152476.3:c.30+460=	NM_152476.3:c.30+449_30+460del	NM_152476.3:c.30+450_30+460del	NM_152476.3:c.30+451_30+460del	NM_152476.3:c.30+452_30+460del	NM_152476.3:c.30+453_30+460del	NM_152476.3:c.30+454_30+460del	NM_152476.3:c.30+455_30+460del	NM_152476.3:c.30+456_30+460del	NM_152476.3:c.30+457_30+460del	NM_152476.3:c.30+458_30+460del	NM_152476.3:c.30+459_30+460del	NM_152476.3:c.30+460del	NM_152476.3:c.30+460dup	NM_152476.3:c.30+459_30+460dup	NM_152476.3:c.30+458_30+460dup	NM_152476.3:c.30+457_30+460dup	NM_152476.3:c.30+456_30+460dup	NM_152476.3:c.30+455_30+460dup	NM_152476.3:c.30+454_30+460dup	NM_152476.3:c.30+453_30+460dup	NM_152476.3:c.30+451_30+460dup	NM_152476.3:c.30+450_30+460dup	NM_152476.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152476.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 transcript variant X3	XM_011527696.3:c.30+460=	XM_011527696.3:c.30+449_30+460del	XM_011527696.3:c.30+450_30+460del	XM_011527696.3:c.30+451_30+460del	XM_011527696.3:c.30+452_30+460del	XM_011527696.3:c.30+453_30+460del	XM_011527696.3:c.30+454_30+460del	XM_011527696.3:c.30+455_30+460del	XM_011527696.3:c.30+456_30+460del	XM_011527696.3:c.30+457_30+460del	XM_011527696.3:c.30+458_30+460del	XM_011527696.3:c.30+459_30+460del	XM_011527696.3:c.30+460del	XM_011527696.3:c.30+460dup	XM_011527696.3:c.30+459_30+460dup	XM_011527696.3:c.30+458_30+460dup	XM_011527696.3:c.30+457_30+460dup	XM_011527696.3:c.30+456_30+460dup	XM_011527696.3:c.30+455_30+460dup	XM_011527696.3:c.30+454_30+460dup	XM_011527696.3:c.30+453_30+460dup	XM_011527696.3:c.30+451_30+460dup	XM_011527696.3:c.30+450_30+460dup	XM_011527696.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527696.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527696.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527696.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527696.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527696.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ZNF560 transcript variant X2	XM_011527697.3:c.30+460=	XM_011527697.3:c.30+449_30+460del	XM_011527697.3:c.30+450_30+460del	XM_011527697.3:c.30+451_30+460del	XM_011527697.3:c.30+452_30+460del	XM_011527697.3:c.30+453_30+460del	XM_011527697.3:c.30+454_30+460del	XM_011527697.3:c.30+455_30+460del	XM_011527697.3:c.30+456_30+460del	XM_011527697.3:c.30+457_30+460del	XM_011527697.3:c.30+458_30+460del	XM_011527697.3:c.30+459_30+460del	XM_011527697.3:c.30+460del	XM_011527697.3:c.30+460dup	XM_011527697.3:c.30+459_30+460dup	XM_011527697.3:c.30+458_30+460dup	XM_011527697.3:c.30+457_30+460dup	XM_011527697.3:c.30+456_30+460dup	XM_011527697.3:c.30+455_30+460dup	XM_011527697.3:c.30+454_30+460dup	XM_011527697.3:c.30+453_30+460dup	XM_011527697.3:c.30+451_30+460dup	XM_011527697.3:c.30+450_30+460dup	XM_011527697.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527697.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527697.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527697.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527697.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011527697.3:c.30+460_30+461insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

61 SubSNP, 44 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40976905	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss96277791	Oct 12, 2018 (152)
3	PJP	ss294953589	Oct 12, 2018 (152)
4	EVA_UK10K_ALSPAC	ss1709118061	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1709118062	Apr 01, 2015 (144)
6	SWEGEN	ss3017085011	Nov 08, 2017 (151)
7	PACBIO	ss3788466343	Jul 13, 2019 (153)
8	PACBIO	ss3793386931	Jul 13, 2019 (153)
9	PACBIO	ss3793386932	Jul 13, 2019 (153)
10	PACBIO	ss3798273582	Jul 13, 2019 (153)
11	PACBIO	ss3798273583	Jul 13, 2019 (153)
12	EVA	ss3835348148	Apr 27, 2020 (154)
13	KOGIC	ss3980817180	Apr 27, 2020 (154)
14	KOGIC	ss3980817181	Apr 27, 2020 (154)
15	KOGIC	ss3980817182	Apr 27, 2020 (154)
16	KOGIC	ss3980817183	Apr 27, 2020 (154)
17	KOGIC	ss3980817184	Apr 27, 2020 (154)
18	GNOMAD	ss4327515903	Apr 27, 2021 (155)
19	GNOMAD	ss4327515904	Apr 27, 2021 (155)
20	GNOMAD	ss4327515905	Apr 27, 2021 (155)
21	GNOMAD	ss4327515906	Apr 27, 2021 (155)
22	GNOMAD	ss4327515907	Apr 27, 2021 (155)
23	GNOMAD	ss4327515908	Apr 27, 2021 (155)
24	GNOMAD	ss4327515909	Apr 27, 2021 (155)
25	GNOMAD	ss4327515910	Apr 27, 2021 (155)
26	GNOMAD	ss4327515911	Apr 27, 2021 (155)
27	GNOMAD	ss4327515912	Apr 27, 2021 (155)
28	GNOMAD	ss4327515913	Apr 27, 2021 (155)
29	GNOMAD	ss4327515914	Apr 27, 2021 (155)
30	GNOMAD	ss4327515916	Apr 27, 2021 (155)
31	GNOMAD	ss4327515917	Apr 27, 2021 (155)
32	GNOMAD	ss4327515918	Apr 27, 2021 (155)
33	GNOMAD	ss4327515919	Apr 27, 2021 (155)
34	GNOMAD	ss4327515920	Apr 27, 2021 (155)
35	GNOMAD	ss4327515921	Apr 27, 2021 (155)
36	GNOMAD	ss4327515922	Apr 27, 2021 (155)
37	GNOMAD	ss4327515923	Apr 27, 2021 (155)
38	GNOMAD	ss4327515924	Apr 27, 2021 (155)
39	GNOMAD	ss4327515925	Apr 27, 2021 (155)
40	GNOMAD	ss4327515926	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5226703311	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5226703312	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5226703313	Apr 27, 2021 (155)
44	TOMMO_GENOMICS	ss5226703314	Apr 27, 2021 (155)
45	TOMMO_GENOMICS	ss5226703315	Apr 27, 2021 (155)
46	TOMMO_GENOMICS	ss5226703316	Apr 27, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5306465299	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5306465300	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5306465301	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5499098081	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5499098082	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5499098083	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5499098084	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5499098085	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5784970021	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5784970022	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5784970023	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5784970024	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5784970025	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5784970026	Oct 16, 2022 (156)
61	EVA	ss5953384093	Oct 16, 2022 (156)
62	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 9585500	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 533837480 (NC_000019.10:9474823::T 25227/80328) Row 533837481 (NC_000019.10:9474823::TTTTT 276/79668) Row 533837482 (NC_000019.10:9474823::TTTTTT 39/79660)...	-	Apr 27, 2021 (155)
87	Korean Genome Project Submission ignored due to conflicting rows: Row 37195181 (NC_000019.10:9474824::TT 259/1826) Row 37195182 (NC_000019.10:9474824::T 532/1826) Row 37195183 (NC_000019.10:9474824::TTTT 36/1826)...	-	Apr 27, 2020 (154)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 37195181 (NC_000019.10:9474824::TT 259/1826) Row 37195182 (NC_000019.10:9474824::T 532/1826) Row 37195183 (NC_000019.10:9474824::TTTT 36/1826)...	-	Apr 27, 2020 (154)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 37195181 (NC_000019.10:9474824::TT 259/1826) Row 37195182 (NC_000019.10:9474824::T 532/1826) Row 37195183 (NC_000019.10:9474824::TTTT 36/1826)...	-	Apr 27, 2020 (154)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 37195181 (NC_000019.10:9474824::TT 259/1826) Row 37195182 (NC_000019.10:9474824::T 532/1826) Row 37195183 (NC_000019.10:9474824::TTTT 36/1826)...	-	Apr 27, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 37195181 (NC_000019.10:9474824::TT 259/1826) Row 37195182 (NC_000019.10:9474824::T 532/1826) Row 37195183 (NC_000019.10:9474824::TTTT 36/1826)...	-	Apr 27, 2020 (154)
92	8.3KJPN Submission ignored due to conflicting rows: Row 84672618 (NC_000019.9:9585499::T 4799/16638) Row 84672619 (NC_000019.9:9585499::TT 1159/16638) Row 84672620 (NC_000019.9:9585499:T: 323/16638)...	-	Apr 27, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 84672618 (NC_000019.9:9585499::T 4799/16638) Row 84672619 (NC_000019.9:9585499::TT 1159/16638) Row 84672620 (NC_000019.9:9585499:T: 323/16638)...	-	Apr 27, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 84672618 (NC_000019.9:9585499::T 4799/16638) Row 84672619 (NC_000019.9:9585499::TT 1159/16638) Row 84672620 (NC_000019.9:9585499:T: 323/16638)...	-	Apr 27, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 84672618 (NC_000019.9:9585499::T 4799/16638) Row 84672619 (NC_000019.9:9585499::TT 1159/16638) Row 84672620 (NC_000019.9:9585499:T: 323/16638)...	-	Apr 27, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 84672618 (NC_000019.9:9585499::T 4799/16638) Row 84672619 (NC_000019.9:9585499::TT 1159/16638) Row 84672620 (NC_000019.9:9585499:T: 323/16638)...	-	Apr 27, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 84672618 (NC_000019.9:9585499::T 4799/16638) Row 84672619 (NC_000019.9:9585499::TT 1159/16638) Row 84672620 (NC_000019.9:9585499:T: 323/16638)...	-	Apr 27, 2021 (155)
98	14KJPN Submission ignored due to conflicting rows: Row 118807125 (NC_000019.10:9474823::T 7880/27994) Row 118807126 (NC_000019.10:9474823::TT 2024/27994) Row 118807127 (NC_000019.10:9474823:T: 710/27994)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 118807125 (NC_000019.10:9474823::T 7880/27994) Row 118807126 (NC_000019.10:9474823::TT 2024/27994) Row 118807127 (NC_000019.10:9474823:T: 710/27994)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 118807125 (NC_000019.10:9474823::T 7880/27994) Row 118807126 (NC_000019.10:9474823::TT 2024/27994) Row 118807127 (NC_000019.10:9474823:T: 710/27994)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 118807125 (NC_000019.10:9474823::T 7880/27994) Row 118807126 (NC_000019.10:9474823::TT 2024/27994) Row 118807127 (NC_000019.10:9474823:T: 710/27994)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 118807125 (NC_000019.10:9474823::T 7880/27994) Row 118807126 (NC_000019.10:9474823::TT 2024/27994) Row 118807127 (NC_000019.10:9474823:T: 710/27994)...	-	Oct 16, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 118807125 (NC_000019.10:9474823::T 7880/27994) Row 118807126 (NC_000019.10:9474823::TT 2024/27994) Row 118807127 (NC_000019.10:9474823:T: 710/27994)...	-	Oct 16, 2022 (156)
104	UK 10K study - Twins	NC_000019.9 - 9585500	Oct 12, 2018 (152)
105	ALFA	NC_000019.10 - 9474824	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4327515926	NC_000019.10:9474823:TTTTTTTTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4327515925	NC_000019.10:9474823:TTTTTTTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4327515924	NC_000019.10:9474823:TTTTTTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4327515923	NC_000019.10:9474823:TTTTTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4327515922	NC_000019.10:9474823:TTTTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4327515921	NC_000019.10:9474823:TTTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4327515920	NC_000019.10:9474823:TTTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4327515919, ss5306465301, ss5499098085	NC_000019.10:9474823:TTTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4327515918	NC_000019.10:9474823:TTT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5226703316	NC_000019.9:9585499:TT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515917, ss5784970026	NC_000019.10:9474823:TT:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3017085011, ss3793386931, ss3798273582, ss5226703313	NC_000019.9:9585499:T:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3980817184, ss4327515916, ss5499098081, ss5784970023	NC_000019.10:9474823:T:	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294953589	NC_000019.8:9446523::T	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
41943945, 41943945, ss1709118061, ss1709118062, ss3835348148, ss5226703311, ss5953384093	NC_000019.9:9585499::T	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515903, ss5306465299, ss5499098082, ss5784970021	NC_000019.10:9474823::T	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3980817181	NC_000019.10:9474824::T	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss40976905	NT_011295.11:848301::T	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss96277791	NT_011295.11:848325::T	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3788466343, ss3793386932, ss3798273583, ss5226703312	NC_000019.9:9585499::TT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5306465300, ss5499098083, ss5784970022	NC_000019.10:9474823::TT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3980817180	NC_000019.10:9474824::TT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5226703314	NC_000019.9:9585499::TTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5499098084, ss5784970024	NC_000019.10:9474823::TTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3980817183	NC_000019.10:9474824::TTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5226703315	NC_000019.9:9585499::TTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5784970025	NC_000019.10:9474823::TTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3980817182	NC_000019.10:9474824::TTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515904	NC_000019.10:9474823::TTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515905	NC_000019.10:9474823::TTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515906	NC_000019.10:9474823::TTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14887102481	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515907	NC_000019.10:9474823::TTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515908	NC_000019.10:9474823::TTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515909	NC_000019.10:9474823::TTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515910	NC_000019.10:9474823::TTTTTTTTTTTT… NC_000019.10:9474823::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515911	NC_000019.10:9474823::TTTTTTTTTTTT… NC_000019.10:9474823::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515912	NC_000019.10:9474823::TTTTTTTTTTTT… NC_000019.10:9474823::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515913	NC_000019.10:9474823::TTTTTTTTTTTT… NC_000019.10:9474823::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327515914	NC_000019.10:9474823::TTTTTTTTTTTT… NC_000019.10:9474823::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000019.10:9474823::TTTTTTTTTTTT… NC_000019.10:9474823::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:9474823:TTTTTTTTTTTTT… NC_000019.10:9474823:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs35450965

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35450965