Name: rs567439951
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.

rs567439951

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:12332348-12332364 (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)₈ / del(T)₇ / del(T)₆ / del(…
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)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₁ / ins(T)₂₀
Variation Type: Indel Insertion and Deletion
Frequency: delTTT=0.000004 (1/264690, TOPMED)
dupT=0.00349 (52/14882, ALFA)
delT=0.1248 (625/5008, 1000G) (+ 1 more)
dupT=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF563 : 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	14882	TTTTTTTTTTTTTTTTT=0.99180	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00255, TTTTTTTTTTTTTTTTTT=0.00349, TTTTTTTTTTTTTTTTTTTTTTTT=0.00215, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	0.993488	0.000407	0.006105	32
European	Sub	11584	TTTTTTTTTTTTTTTTT=0.98947	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00328, TTTTTTTTTTTTTTTTTT=0.00449, TTTTTTTTTTTTTTTTTTTTTTTT=0.00276, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	0.991611	0.000524	0.007864	32
African	Sub	1966	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	74	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1892	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	108	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	122	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	582	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	88	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	432	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₁₇=0.999996	delTTT=0.000004
Allele Frequency Aggregator	Total	Global	14882	(T)₁₇=0.99180	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00255, dupT=0.00349, dupTT=0.00000, dupTTT=0.00000, dup(T)₇=0.00215
Allele Frequency Aggregator	European	Sub	11584	(T)₁₇=0.98947	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00328, dupT=0.00449, dupTT=0.00000, dupTTT=0.00000, dup(T)₇=0.00276
Allele Frequency Aggregator	African	Sub	1966	(T)₁₇=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	582	(T)₁₇=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	432	(T)₁₇=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	122	(T)₁₇=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Asian	Sub	108	(T)₁₇=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(T)₁₇=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₇=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₇=0.8752	delT=0.1248
1000Genomes	African	Sub	1322	(T)₁₇=0.8018	delT=0.1982
1000Genomes	East Asian	Sub	1008	(T)₁₇=0.9375	delT=0.0625
1000Genomes	Europe	Sub	1006	(T)₁₇=0.8767	delT=0.1233
1000Genomes	South Asian	Sub	978	(T)₁₇=0.937	delT=0.063
1000Genomes	American	Sub	694	(T)₁₇=0.836	delT=0.164
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.25

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.12332357_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332358_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332359_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332360_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332361_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332362_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332363_12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332364del
GRCh38.p14 chr 19	NC_000019.10:g.12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332363_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332362_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332361_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332359_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332358_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332357_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332356_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332354_12332364dup
GRCh38.p14 chr 19	NC_000019.10:g.12332364_12332365insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.12443171_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443172_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443173_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443174_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443175_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443176_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443177_12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443178del
GRCh37.p13 chr 19	NC_000019.9:g.12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443177_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443176_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443175_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443173_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443172_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443171_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443170_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443168_12443178dup
GRCh37.p13 chr 19	NC_000019.9:g.12443178_12443179insTTTTTTTTTTTTTTTTTTTT

Gene: ZNF563, zinc finger protein 563 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF563 transcript variant 2	NM_001363608.1:c.3+1125_3… NM_001363608.1:c.3+1125_3+1132del	N/A	Intron Variant
ZNF563 transcript variant 1	NM_145276.3:c.3+1125_3+11… NM_145276.3:c.3+1125_3+1132del	N/A	Intron Variant
ZNF563 transcript variant X5	XM_005259750.5:c.3+1125_3… XM_005259750.5:c.3+1125_3+1132del	N/A	Intron Variant
ZNF563 transcript variant X4	XM_006722651.4:c.3+1125_3… XM_006722651.4:c.3+1125_3+1132del	N/A	Intron Variant
ZNF563 transcript variant X2	XM_011527700.3:c.-47-9644… XM_011527700.3:c.-47-9644_-47-9637del	N/A	Intron Variant
ZNF563 transcript variant X1	XM_011527698.3:c.	N/A	Genic Upstream Transcript Variant
ZNF563 transcript variant X3	XM_011527699.3:c.	N/A	Genic Upstream Transcript 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)₁₇=	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)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₁	ins(T)₂₀
GRCh38.p14 chr 19	NC_000019.10:g.12332348_12332364=	NC_000019.10:g.12332357_12332364del	NC_000019.10:g.12332358_12332364del	NC_000019.10:g.12332359_12332364del	NC_000019.10:g.12332360_12332364del	NC_000019.10:g.12332361_12332364del	NC_000019.10:g.12332362_12332364del	NC_000019.10:g.12332363_12332364del	NC_000019.10:g.12332364del	NC_000019.10:g.12332364dup	NC_000019.10:g.12332363_12332364dup	NC_000019.10:g.12332362_12332364dup	NC_000019.10:g.12332361_12332364dup	NC_000019.10:g.12332359_12332364dup	NC_000019.10:g.12332358_12332364dup	NC_000019.10:g.12332357_12332364dup	NC_000019.10:g.12332356_12332364dup	NC_000019.10:g.12332354_12332364dup	NC_000019.10:g.12332364_12332365insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.12443162_12443178=	NC_000019.9:g.12443171_12443178del	NC_000019.9:g.12443172_12443178del	NC_000019.9:g.12443173_12443178del	NC_000019.9:g.12443174_12443178del	NC_000019.9:g.12443175_12443178del	NC_000019.9:g.12443176_12443178del	NC_000019.9:g.12443177_12443178del	NC_000019.9:g.12443178del	NC_000019.9:g.12443178dup	NC_000019.9:g.12443177_12443178dup	NC_000019.9:g.12443176_12443178dup	NC_000019.9:g.12443175_12443178dup	NC_000019.9:g.12443173_12443178dup	NC_000019.9:g.12443172_12443178dup	NC_000019.9:g.12443171_12443178dup	NC_000019.9:g.12443170_12443178dup	NC_000019.9:g.12443168_12443178dup	NC_000019.9:g.12443178_12443179insTTTTTTTTTTTTTTTTTTTT
ZNF563 transcript variant 2	NM_001363608.1:c.3+1132=	NM_001363608.1:c.3+1125_3+1132del	NM_001363608.1:c.3+1126_3+1132del	NM_001363608.1:c.3+1127_3+1132del	NM_001363608.1:c.3+1128_3+1132del	NM_001363608.1:c.3+1129_3+1132del	NM_001363608.1:c.3+1130_3+1132del	NM_001363608.1:c.3+1131_3+1132del	NM_001363608.1:c.3+1132del	NM_001363608.1:c.3+1132dup	NM_001363608.1:c.3+1131_3+1132dup	NM_001363608.1:c.3+1130_3+1132dup	NM_001363608.1:c.3+1129_3+1132dup	NM_001363608.1:c.3+1127_3+1132dup	NM_001363608.1:c.3+1126_3+1132dup	NM_001363608.1:c.3+1125_3+1132dup	NM_001363608.1:c.3+1124_3+1132dup	NM_001363608.1:c.3+1122_3+1132dup	NM_001363608.1:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant 1	NM_145276.2:c.3+1132=	NM_145276.2:c.3+1125_3+1132del	NM_145276.2:c.3+1126_3+1132del	NM_145276.2:c.3+1127_3+1132del	NM_145276.2:c.3+1128_3+1132del	NM_145276.2:c.3+1129_3+1132del	NM_145276.2:c.3+1130_3+1132del	NM_145276.2:c.3+1131_3+1132del	NM_145276.2:c.3+1132del	NM_145276.2:c.3+1132dup	NM_145276.2:c.3+1131_3+1132dup	NM_145276.2:c.3+1130_3+1132dup	NM_145276.2:c.3+1129_3+1132dup	NM_145276.2:c.3+1127_3+1132dup	NM_145276.2:c.3+1126_3+1132dup	NM_145276.2:c.3+1125_3+1132dup	NM_145276.2:c.3+1124_3+1132dup	NM_145276.2:c.3+1122_3+1132dup	NM_145276.2:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant 1	NM_145276.3:c.3+1132=	NM_145276.3:c.3+1125_3+1132del	NM_145276.3:c.3+1126_3+1132del	NM_145276.3:c.3+1127_3+1132del	NM_145276.3:c.3+1128_3+1132del	NM_145276.3:c.3+1129_3+1132del	NM_145276.3:c.3+1130_3+1132del	NM_145276.3:c.3+1131_3+1132del	NM_145276.3:c.3+1132del	NM_145276.3:c.3+1132dup	NM_145276.3:c.3+1131_3+1132dup	NM_145276.3:c.3+1130_3+1132dup	NM_145276.3:c.3+1129_3+1132dup	NM_145276.3:c.3+1127_3+1132dup	NM_145276.3:c.3+1126_3+1132dup	NM_145276.3:c.3+1125_3+1132dup	NM_145276.3:c.3+1124_3+1132dup	NM_145276.3:c.3+1122_3+1132dup	NM_145276.3:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X1	XM_005259748.1:c.3+1132=	XM_005259748.1:c.3+1125_3+1132del	XM_005259748.1:c.3+1126_3+1132del	XM_005259748.1:c.3+1127_3+1132del	XM_005259748.1:c.3+1128_3+1132del	XM_005259748.1:c.3+1129_3+1132del	XM_005259748.1:c.3+1130_3+1132del	XM_005259748.1:c.3+1131_3+1132del	XM_005259748.1:c.3+1132del	XM_005259748.1:c.3+1132dup	XM_005259748.1:c.3+1131_3+1132dup	XM_005259748.1:c.3+1130_3+1132dup	XM_005259748.1:c.3+1129_3+1132dup	XM_005259748.1:c.3+1127_3+1132dup	XM_005259748.1:c.3+1126_3+1132dup	XM_005259748.1:c.3+1125_3+1132dup	XM_005259748.1:c.3+1124_3+1132dup	XM_005259748.1:c.3+1122_3+1132dup	XM_005259748.1:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X2	XM_005259749.1:c.3+1132=	XM_005259749.1:c.3+1125_3+1132del	XM_005259749.1:c.3+1126_3+1132del	XM_005259749.1:c.3+1127_3+1132del	XM_005259749.1:c.3+1128_3+1132del	XM_005259749.1:c.3+1129_3+1132del	XM_005259749.1:c.3+1130_3+1132del	XM_005259749.1:c.3+1131_3+1132del	XM_005259749.1:c.3+1132del	XM_005259749.1:c.3+1132dup	XM_005259749.1:c.3+1131_3+1132dup	XM_005259749.1:c.3+1130_3+1132dup	XM_005259749.1:c.3+1129_3+1132dup	XM_005259749.1:c.3+1127_3+1132dup	XM_005259749.1:c.3+1126_3+1132dup	XM_005259749.1:c.3+1125_3+1132dup	XM_005259749.1:c.3+1124_3+1132dup	XM_005259749.1:c.3+1122_3+1132dup	XM_005259749.1:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X3	XM_005259750.1:c.3+1132=	XM_005259750.1:c.3+1125_3+1132del	XM_005259750.1:c.3+1126_3+1132del	XM_005259750.1:c.3+1127_3+1132del	XM_005259750.1:c.3+1128_3+1132del	XM_005259750.1:c.3+1129_3+1132del	XM_005259750.1:c.3+1130_3+1132del	XM_005259750.1:c.3+1131_3+1132del	XM_005259750.1:c.3+1132del	XM_005259750.1:c.3+1132dup	XM_005259750.1:c.3+1131_3+1132dup	XM_005259750.1:c.3+1130_3+1132dup	XM_005259750.1:c.3+1129_3+1132dup	XM_005259750.1:c.3+1127_3+1132dup	XM_005259750.1:c.3+1126_3+1132dup	XM_005259750.1:c.3+1125_3+1132dup	XM_005259750.1:c.3+1124_3+1132dup	XM_005259750.1:c.3+1122_3+1132dup	XM_005259750.1:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X5	XM_005259750.5:c.3+1132=	XM_005259750.5:c.3+1125_3+1132del	XM_005259750.5:c.3+1126_3+1132del	XM_005259750.5:c.3+1127_3+1132del	XM_005259750.5:c.3+1128_3+1132del	XM_005259750.5:c.3+1129_3+1132del	XM_005259750.5:c.3+1130_3+1132del	XM_005259750.5:c.3+1131_3+1132del	XM_005259750.5:c.3+1132del	XM_005259750.5:c.3+1132dup	XM_005259750.5:c.3+1131_3+1132dup	XM_005259750.5:c.3+1130_3+1132dup	XM_005259750.5:c.3+1129_3+1132dup	XM_005259750.5:c.3+1127_3+1132dup	XM_005259750.5:c.3+1126_3+1132dup	XM_005259750.5:c.3+1125_3+1132dup	XM_005259750.5:c.3+1124_3+1132dup	XM_005259750.5:c.3+1122_3+1132dup	XM_005259750.5:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X4	XM_005259751.1:c.3+1132=	XM_005259751.1:c.3+1125_3+1132del	XM_005259751.1:c.3+1126_3+1132del	XM_005259751.1:c.3+1127_3+1132del	XM_005259751.1:c.3+1128_3+1132del	XM_005259751.1:c.3+1129_3+1132del	XM_005259751.1:c.3+1130_3+1132del	XM_005259751.1:c.3+1131_3+1132del	XM_005259751.1:c.3+1132del	XM_005259751.1:c.3+1132dup	XM_005259751.1:c.3+1131_3+1132dup	XM_005259751.1:c.3+1130_3+1132dup	XM_005259751.1:c.3+1129_3+1132dup	XM_005259751.1:c.3+1127_3+1132dup	XM_005259751.1:c.3+1126_3+1132dup	XM_005259751.1:c.3+1125_3+1132dup	XM_005259751.1:c.3+1124_3+1132dup	XM_005259751.1:c.3+1122_3+1132dup	XM_005259751.1:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X5	XM_005259752.1:c.3+1132=	XM_005259752.1:c.3+1125_3+1132del	XM_005259752.1:c.3+1126_3+1132del	XM_005259752.1:c.3+1127_3+1132del	XM_005259752.1:c.3+1128_3+1132del	XM_005259752.1:c.3+1129_3+1132del	XM_005259752.1:c.3+1130_3+1132del	XM_005259752.1:c.3+1131_3+1132del	XM_005259752.1:c.3+1132del	XM_005259752.1:c.3+1132dup	XM_005259752.1:c.3+1131_3+1132dup	XM_005259752.1:c.3+1130_3+1132dup	XM_005259752.1:c.3+1129_3+1132dup	XM_005259752.1:c.3+1127_3+1132dup	XM_005259752.1:c.3+1126_3+1132dup	XM_005259752.1:c.3+1125_3+1132dup	XM_005259752.1:c.3+1124_3+1132dup	XM_005259752.1:c.3+1122_3+1132dup	XM_005259752.1:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X4	XM_006722651.4:c.3+1132=	XM_006722651.4:c.3+1125_3+1132del	XM_006722651.4:c.3+1126_3+1132del	XM_006722651.4:c.3+1127_3+1132del	XM_006722651.4:c.3+1128_3+1132del	XM_006722651.4:c.3+1129_3+1132del	XM_006722651.4:c.3+1130_3+1132del	XM_006722651.4:c.3+1131_3+1132del	XM_006722651.4:c.3+1132del	XM_006722651.4:c.3+1132dup	XM_006722651.4:c.3+1131_3+1132dup	XM_006722651.4:c.3+1130_3+1132dup	XM_006722651.4:c.3+1129_3+1132dup	XM_006722651.4:c.3+1127_3+1132dup	XM_006722651.4:c.3+1126_3+1132dup	XM_006722651.4:c.3+1125_3+1132dup	XM_006722651.4:c.3+1124_3+1132dup	XM_006722651.4:c.3+1122_3+1132dup	XM_006722651.4:c.3+1132_3+1133insAAAAAAAAAAAAAAAAAAAA
ZNF563 transcript variant X2	XM_011527700.3:c.-47-9637=	XM_011527700.3:c.-47-9644_-47-9637del	XM_011527700.3:c.-47-9643_-47-9637del	XM_011527700.3:c.-47-9642_-47-9637del	XM_011527700.3:c.-47-9641_-47-9637del	XM_011527700.3:c.-47-9640_-47-9637del	XM_011527700.3:c.-47-9639_-47-9637del	XM_011527700.3:c.-47-9638_-47-9637del	XM_011527700.3:c.-47-9637del	XM_011527700.3:c.-47-9637dup	XM_011527700.3:c.-47-9638_-47-9637dup	XM_011527700.3:c.-47-9639_-47-9637dup	XM_011527700.3:c.-47-9640_-47-9637dup	XM_011527700.3:c.-47-9642_-47-9637dup	XM_011527700.3:c.-47-9643_-47-9637dup	XM_011527700.3:c.-47-9644_-47-9637dup	XM_011527700.3:c.-47-9645_-47-9637dup	XM_011527700.3:c.-47-9647_-47-9637dup	XM_011527700.3:c.-47-9637_-47-9636insAAAAAAAAAAAAAAAAAAAA

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#.

38 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss1377972355	Aug 21, 2014 (142)
2	EVA_GENOME_DK	ss1575240541	Apr 01, 2015 (144)
3	SWEGEN	ss3017124104	Nov 08, 2017 (151)
4	PACBIO	ss3788472317	Jul 13, 2019 (153)
5	KHV_HUMAN_GENOMES	ss3821083197	Jul 13, 2019 (153)
6	GNOMAD	ss4327902423	Apr 26, 2021 (155)
7	GNOMAD	ss4327902424	Apr 26, 2021 (155)
8	GNOMAD	ss4327902425	Apr 26, 2021 (155)
9	GNOMAD	ss4327902426	Apr 26, 2021 (155)
10	GNOMAD	ss4327902427	Apr 26, 2021 (155)
11	GNOMAD	ss4327902428	Apr 26, 2021 (155)
12	GNOMAD	ss4327902429	Apr 26, 2021 (155)
13	GNOMAD	ss4327902430	Apr 26, 2021 (155)
14	GNOMAD	ss4327902431	Apr 26, 2021 (155)
15	GNOMAD	ss4327902432	Apr 26, 2021 (155)
16	GNOMAD	ss4327902433	Apr 26, 2021 (155)
17	GNOMAD	ss4327902434	Apr 26, 2021 (155)
18	GNOMAD	ss4327902435	Apr 26, 2021 (155)
19	GNOMAD	ss4327902436	Apr 26, 2021 (155)
20	GNOMAD	ss4327902437	Apr 26, 2021 (155)
21	GNOMAD	ss4327902438	Apr 26, 2021 (155)
22	TOPMED	ss5068438584	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5226815653	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5226815654	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5226815655	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5306548564	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5306548565	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5306548566	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5306548567	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5499169730	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5499169731	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5499169732	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5499169733	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5499169734	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5785121605	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5785121607	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5785121608	Oct 16, 2022 (156)
38	YY_MCH	ss5817420681	Oct 16, 2022 (156)
39	1000Genomes	NC_000019.9 - 12443162	Oct 12, 2018 (152)
40	The Danish reference pan genome	NC_000019.9 - 12443162	Apr 27, 2020 (154)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534486714 (NC_000019.10:12332347::T 3223/124052) Row 534486715 (NC_000019.10:12332347::TT 1054/124094) Row 534486716 (NC_000019.10:12332347::TTT 9/124130)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 84784960 (NC_000019.9:12443161:TTTTTTT: 4/16754) Row 84784961 (NC_000019.9:12443161::T 75/16754) Row 84784962 (NC_000019.9:12443161:T: 11/16754)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 84784960 (NC_000019.9:12443161:TTTTTTT: 4/16754) Row 84784961 (NC_000019.9:12443161::T 75/16754) Row 84784962 (NC_000019.9:12443161:T: 11/16754)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 84784960 (NC_000019.9:12443161:TTTTTTT: 4/16754) Row 84784961 (NC_000019.9:12443161::T 75/16754) Row 84784962 (NC_000019.9:12443161:T: 11/16754)	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 118958709 (NC_000019.10:12332347:TTTTTTT: 12/28258) Row 118958711 (NC_000019.10:12332347:T: 16/28258) Row 118958712 (NC_000019.10:12332347::T 162/28258)	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 118958709 (NC_000019.10:12332347:TTTTTTT: 12/28258) Row 118958711 (NC_000019.10:12332347:T: 16/28258) Row 118958712 (NC_000019.10:12332347::T 162/28258)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 118958709 (NC_000019.10:12332347:TTTTTTT: 12/28258) Row 118958711 (NC_000019.10:12332347:T: 16/28258) Row 118958712 (NC_000019.10:12332347::T 162/28258)	-	Oct 16, 2022 (156)
63	TopMed	NC_000019.10 - 12332348	Apr 26, 2021 (155)
64	ALFA	NC_000019.10 - 12332348	Apr 26, 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
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss5226815653	NC_000019.9:12443161:TTTTTTT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4327902438, ss5306548566, ss5499169734, ss5785121605	NC_000019.10:12332347:TTTTTTT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4327902437	NC_000019.10:12332347:TTTTTT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4327902436	NC_000019.10:12332347:TTTTT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4327902435	NC_000019.10:12332347:TTTT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
283984248, ss4327902434, ss5068438584	NC_000019.10:12332347:TTT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4327902433, ss5499169732	NC_000019.10:12332347:TT:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
75787453, ss1377972355, ss3017124104, ss3788472317, ss5226815655	NC_000019.9:12443161:T:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3821083197, ss4327902432, ss5306548564, ss5499169731, ss5785121607	NC_000019.10:12332347:T:	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
620946, ss1575240541, ss5226815654	NC_000019.9:12443161::T	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4327902423, ss5306548567, ss5499169730, ss5785121608, ss5817420681	NC_000019.10:12332347::T	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4327902424, ss5306548565, ss5499169733	NC_000019.10:12332347::TT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4327902425	NC_000019.10:12332347::TTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4327902426	NC_000019.10:12332347::TTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4327902427	NC_000019.10:12332347::TTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2897776816	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327902428	NC_000019.10:12332347::TTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327902429	NC_000019.10:12332347::TTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327902430	NC_000019.10:12332347::TTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327902431	NC_000019.10:12332347::TTTTTTTTTTT… NC_000019.10:12332347::TTTTTTTTTTTTTTTTTTTT	NC_000019.10:12332347:TTTTTTTTTTTT… NC_000019.10:12332347:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs567439951

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

rs567439951