Name: rs34389091
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.

rs34389091

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:17427298-17427322 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / 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)₉ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / ins(T)₃₆
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.1142 (657/5752, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02217 : 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	5752	TTTTTTTTTTTTTTTTTTTTTTTTT=0.7283	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=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=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.1010, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0320, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1142, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0214, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0014	0.873596	0.08661	0.039794	32
European	Sub	5176	TTTTTTTTTTTTTTTTTTTTTTTTT=0.6988	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=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=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.1121, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0354, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1265, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0238, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0015	0.854516	0.099513	0.045971	32
African	Sub	422	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	406	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	14	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	34	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	66	TTTTTTTTTTTTTTTTTTTTTTTTT=0.94	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.96875	0.03125	0.0	17

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
Allele Frequency Aggregator	Total	Global	5752	(T)₂₅=0.7283	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=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=0.1010, dupT=0.0320, dupTT=0.1142, dupTTT=0.0214, dup(T)₄=0.0017, ins(T)₃₆=0.0014
Allele Frequency Aggregator	European	Sub	5176	(T)₂₅=0.6988	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=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=0.1121, dupT=0.0354, dupTT=0.1265, dupTTT=0.0238, dup(T)₄=0.0019, ins(T)₃₆=0.0015
Allele Frequency Aggregator	African	Sub	422	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=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, ins(T)₃₆=0.000
Allele Frequency Aggregator	Other	Sub	66	(T)₂₅=0.94	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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=0.02, dupT=0.02, dupTT=0.03, dupTTT=0.00, dup(T)₄=0.00, ins(T)₃₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	34	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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, ins(T)₃₆=0.00
Allele Frequency Aggregator	Asian	Sub	22	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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, ins(T)₃₆=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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, ins(T)₃₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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, ins(T)₃₆=0.00

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 5	NC_000005.10:g.17427309_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427310_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427311_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427312_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427313_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427314_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427315_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427316_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427317_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427318_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427319_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427320_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427321_17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427322del
GRCh38.p14 chr 5	NC_000005.10:g.17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427321_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427320_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427319_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427318_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427317_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427316_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427315_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427314_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427312_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427311_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427310_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427308_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427307_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427306_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427305_17427322dup
GRCh38.p14 chr 5	NC_000005.10:g.17427322_17427323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 5	NC_000005.9:g.17427418_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427419_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427420_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427421_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427422_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427423_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427424_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427425_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427426_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427427_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427428_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427429_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427430_17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427431del
GRCh37.p13 chr 5	NC_000005.9:g.17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427430_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427429_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427428_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427427_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427426_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427425_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427424_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427423_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427421_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427420_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427419_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427417_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427416_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427415_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427414_17427431dup
GRCh37.p13 chr 5	NC_000005.9:g.17427431_17427432insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LINC02217, long intergenic non-protein coding RNA 2217 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02217 transcript variant 2	NR_134274.1:n.	N/A	Intron Variant
LINC02217 transcript variant 3	NR_134275.1:n.	N/A	Intron Variant
LINC02217 transcript variant 1	NR_134273.1:n.	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)₂₅=	del(T)₁₄	del(T)₁₃	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)₉	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	ins(T)₃₆
GRCh38.p14 chr 5	NC_000005.10:g.17427298_17427322=	NC_000005.10:g.17427309_17427322del	NC_000005.10:g.17427310_17427322del	NC_000005.10:g.17427311_17427322del	NC_000005.10:g.17427312_17427322del	NC_000005.10:g.17427313_17427322del	NC_000005.10:g.17427314_17427322del	NC_000005.10:g.17427315_17427322del	NC_000005.10:g.17427316_17427322del	NC_000005.10:g.17427317_17427322del	NC_000005.10:g.17427318_17427322del	NC_000005.10:g.17427319_17427322del	NC_000005.10:g.17427320_17427322del	NC_000005.10:g.17427321_17427322del	NC_000005.10:g.17427322del	NC_000005.10:g.17427322dup	NC_000005.10:g.17427321_17427322dup	NC_000005.10:g.17427320_17427322dup	NC_000005.10:g.17427319_17427322dup	NC_000005.10:g.17427318_17427322dup	NC_000005.10:g.17427317_17427322dup	NC_000005.10:g.17427316_17427322dup	NC_000005.10:g.17427315_17427322dup	NC_000005.10:g.17427314_17427322dup	NC_000005.10:g.17427312_17427322dup	NC_000005.10:g.17427311_17427322dup	NC_000005.10:g.17427310_17427322dup	NC_000005.10:g.17427308_17427322dup	NC_000005.10:g.17427307_17427322dup	NC_000005.10:g.17427306_17427322dup	NC_000005.10:g.17427305_17427322dup	NC_000005.10:g.17427322_17427323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 5	NC_000005.9:g.17427407_17427431=	NC_000005.9:g.17427418_17427431del	NC_000005.9:g.17427419_17427431del	NC_000005.9:g.17427420_17427431del	NC_000005.9:g.17427421_17427431del	NC_000005.9:g.17427422_17427431del	NC_000005.9:g.17427423_17427431del	NC_000005.9:g.17427424_17427431del	NC_000005.9:g.17427425_17427431del	NC_000005.9:g.17427426_17427431del	NC_000005.9:g.17427427_17427431del	NC_000005.9:g.17427428_17427431del	NC_000005.9:g.17427429_17427431del	NC_000005.9:g.17427430_17427431del	NC_000005.9:g.17427431del	NC_000005.9:g.17427431dup	NC_000005.9:g.17427430_17427431dup	NC_000005.9:g.17427429_17427431dup	NC_000005.9:g.17427428_17427431dup	NC_000005.9:g.17427427_17427431dup	NC_000005.9:g.17427426_17427431dup	NC_000005.9:g.17427425_17427431dup	NC_000005.9:g.17427424_17427431dup	NC_000005.9:g.17427423_17427431dup	NC_000005.9:g.17427421_17427431dup	NC_000005.9:g.17427420_17427431dup	NC_000005.9:g.17427419_17427431dup	NC_000005.9:g.17427417_17427431dup	NC_000005.9:g.17427416_17427431dup	NC_000005.9:g.17427415_17427431dup	NC_000005.9:g.17427414_17427431dup	NC_000005.9:g.17427431_17427432insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

70 SubSNP, 53 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82000434	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95387489	Feb 13, 2009 (135)
3	HUMANGENOME_JCVI	ss98672875	Mar 15, 2016 (147)
4	PJP	ss295214707	May 09, 2011 (135)
5	PJP	ss295214708	May 09, 2011 (135)
6	EVA_UK10K_ALSPAC	ss1704581323	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1704581324	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1704581326	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1704581345	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1704581348	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1704581351	Apr 01, 2015 (144)
12	SWEGEN	ss2996515010	Nov 17, 2017 (151)
13	EVA	ss3829119908	Apr 26, 2020 (154)
14	KOGIC	ss3956183687	Apr 26, 2020 (154)
15	KOGIC	ss3956183688	Apr 26, 2020 (154)
16	KOGIC	ss3956183689	Apr 26, 2020 (154)
17	KOGIC	ss3956183690	Apr 26, 2020 (154)
18	KOGIC	ss3956183691	Apr 26, 2020 (154)
19	KOGIC	ss3956183692	Apr 26, 2020 (154)
20	GNOMAD	ss4100112261	Apr 26, 2021 (155)
21	GNOMAD	ss4100112262	Apr 26, 2021 (155)
22	GNOMAD	ss4100112263	Apr 26, 2021 (155)
23	GNOMAD	ss4100112264	Apr 26, 2021 (155)
24	GNOMAD	ss4100112265	Apr 26, 2021 (155)
25	GNOMAD	ss4100112266	Apr 26, 2021 (155)
26	GNOMAD	ss4100112267	Apr 26, 2021 (155)
27	GNOMAD	ss4100112268	Apr 26, 2021 (155)
28	GNOMAD	ss4100112269	Apr 26, 2021 (155)
29	GNOMAD	ss4100112270	Apr 26, 2021 (155)
30	GNOMAD	ss4100112271	Apr 26, 2021 (155)
31	GNOMAD	ss4100112272	Apr 26, 2021 (155)
32	GNOMAD	ss4100112273	Apr 26, 2021 (155)
33	GNOMAD	ss4100112274	Apr 26, 2021 (155)
34	GNOMAD	ss4100112275	Apr 26, 2021 (155)
35	GNOMAD	ss4100112276	Apr 26, 2021 (155)
36	GNOMAD	ss4100112278	Apr 26, 2021 (155)
37	GNOMAD	ss4100112279	Apr 26, 2021 (155)
38	GNOMAD	ss4100112280	Apr 26, 2021 (155)
39	GNOMAD	ss4100112281	Apr 26, 2021 (155)
40	GNOMAD	ss4100112282	Apr 26, 2021 (155)
41	GNOMAD	ss4100112283	Apr 26, 2021 (155)
42	GNOMAD	ss4100112284	Apr 26, 2021 (155)
43	GNOMAD	ss4100112285	Apr 26, 2021 (155)
44	GNOMAD	ss4100112286	Apr 26, 2021 (155)
45	GNOMAD	ss4100112287	Apr 26, 2021 (155)
46	GNOMAD	ss4100112288	Apr 26, 2021 (155)
47	GNOMAD	ss4100112289	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5170597032	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5170597033	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5170597034	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5170597035	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5170597036	Apr 26, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5263049128	Oct 13, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5263049129	Oct 13, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5263049130	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5263049131	Oct 13, 2022 (156)
57	HUGCELL_USP	ss5461380161	Oct 13, 2022 (156)
58	HUGCELL_USP	ss5461380162	Oct 13, 2022 (156)
59	HUGCELL_USP	ss5461380163	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5461380164	Oct 13, 2022 (156)
61	HUGCELL_USP	ss5461380165	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5706331586	Oct 13, 2022 (156)
63	TOMMO_GENOMICS	ss5706331587	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5706331588	Oct 13, 2022 (156)
65	TOMMO_GENOMICS	ss5706331589	Oct 13, 2022 (156)
66	TOMMO_GENOMICS	ss5706331590	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5706331591	Oct 13, 2022 (156)
68	EVA	ss5834587531	Oct 13, 2022 (156)
69	EVA	ss5834587532	Oct 13, 2022 (156)
70	EVA	ss5893194105	Oct 13, 2022 (156)
71	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 14284851 (NC_000005.9:17427406::TTT 526/3854) Row 14284852 (NC_000005.9:17427406::T 1859/3854) Row 14284853 (NC_000005.9:17427406::TT 1419/3854)	-	Oct 12, 2018 (152)
72	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 14284851 (NC_000005.9:17427406::TTT 526/3854) Row 14284852 (NC_000005.9:17427406::T 1859/3854) Row 14284853 (NC_000005.9:17427406::TT 1419/3854)	-	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 14284851 (NC_000005.9:17427406::TTT 526/3854) Row 14284852 (NC_000005.9:17427406::T 1859/3854) Row 14284853 (NC_000005.9:17427406::TT 1419/3854)	-	Oct 12, 2018 (152)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 181314350 (NC_000005.10:17427297::T 6590/73700) Row 181314351 (NC_000005.10:17427297::TT 21497/73948) Row 181314352 (NC_000005.10:17427297::TTT 4133/73798)...	-	Apr 26, 2021 (155)
103	Korean Genome Project Submission ignored due to conflicting rows: Row 12561688 (NC_000005.10:17427298:T: 94/1822) Row 12561689 (NC_000005.10:17427299::TT 368/1822) Row 12561690 (NC_000005.10:17427299::T 207/1822)...	-	Apr 26, 2020 (154)
104	Korean Genome Project Submission ignored due to conflicting rows: Row 12561688 (NC_000005.10:17427298:T: 94/1822) Row 12561689 (NC_000005.10:17427299::TT 368/1822) Row 12561690 (NC_000005.10:17427299::T 207/1822)...	-	Apr 26, 2020 (154)
105	Korean Genome Project Submission ignored due to conflicting rows: Row 12561688 (NC_000005.10:17427298:T: 94/1822) Row 12561689 (NC_000005.10:17427299::TT 368/1822) Row 12561690 (NC_000005.10:17427299::T 207/1822)...	-	Apr 26, 2020 (154)
106	Korean Genome Project Submission ignored due to conflicting rows: Row 12561688 (NC_000005.10:17427298:T: 94/1822) Row 12561689 (NC_000005.10:17427299::TT 368/1822) Row 12561690 (NC_000005.10:17427299::T 207/1822)...	-	Apr 26, 2020 (154)
107	Korean Genome Project Submission ignored due to conflicting rows: Row 12561688 (NC_000005.10:17427298:T: 94/1822) Row 12561689 (NC_000005.10:17427299::TT 368/1822) Row 12561690 (NC_000005.10:17427299::T 207/1822)...	-	Apr 26, 2020 (154)
108	Korean Genome Project Submission ignored due to conflicting rows: Row 12561688 (NC_000005.10:17427298:T: 94/1822) Row 12561689 (NC_000005.10:17427299::TT 368/1822) Row 12561690 (NC_000005.10:17427299::T 207/1822)...	-	Apr 26, 2020 (154)
109	8.3KJPN Submission ignored due to conflicting rows: Row 28566339 (NC_000005.9:17427406::TT 4454/16144) Row 28566340 (NC_000005.9:17427406::T 1423/16144) Row 28566341 (NC_000005.9:17427406:T: 510/16144)...	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 28566339 (NC_000005.9:17427406::TT 4454/16144) Row 28566340 (NC_000005.9:17427406::T 1423/16144) Row 28566341 (NC_000005.9:17427406:T: 510/16144)...	-	Apr 26, 2021 (155)
111	8.3KJPN Submission ignored due to conflicting rows: Row 28566339 (NC_000005.9:17427406::TT 4454/16144) Row 28566340 (NC_000005.9:17427406::T 1423/16144) Row 28566341 (NC_000005.9:17427406:T: 510/16144)...	-	Apr 26, 2021 (155)
112	8.3KJPN Submission ignored due to conflicting rows: Row 28566339 (NC_000005.9:17427406::TT 4454/16144) Row 28566340 (NC_000005.9:17427406::T 1423/16144) Row 28566341 (NC_000005.9:17427406:T: 510/16144)...	-	Apr 26, 2021 (155)
113	8.3KJPN Submission ignored due to conflicting rows: Row 28566339 (NC_000005.9:17427406::TT 4454/16144) Row 28566340 (NC_000005.9:17427406::T 1423/16144) Row 28566341 (NC_000005.9:17427406:T: 510/16144)...	-	Apr 26, 2021 (155)
114	14KJPN Submission ignored due to conflicting rows: Row 40168690 (NC_000005.10:17427297::TT 9355/28126) Row 40168691 (NC_000005.10:17427297::T 3065/28126) Row 40168692 (NC_000005.10:17427297:T: 1148/28126)...	-	Oct 13, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 40168690 (NC_000005.10:17427297::TT 9355/28126) Row 40168691 (NC_000005.10:17427297::T 3065/28126) Row 40168692 (NC_000005.10:17427297:T: 1148/28126)...	-	Oct 13, 2022 (156)
116	14KJPN Submission ignored due to conflicting rows: Row 40168690 (NC_000005.10:17427297::TT 9355/28126) Row 40168691 (NC_000005.10:17427297::T 3065/28126) Row 40168692 (NC_000005.10:17427297:T: 1148/28126)...	-	Oct 13, 2022 (156)
117	14KJPN Submission ignored due to conflicting rows: Row 40168690 (NC_000005.10:17427297::TT 9355/28126) Row 40168691 (NC_000005.10:17427297::T 3065/28126) Row 40168692 (NC_000005.10:17427297:T: 1148/28126)...	-	Oct 13, 2022 (156)
118	14KJPN Submission ignored due to conflicting rows: Row 40168690 (NC_000005.10:17427297::TT 9355/28126) Row 40168691 (NC_000005.10:17427297::T 3065/28126) Row 40168692 (NC_000005.10:17427297:T: 1148/28126)...	-	Oct 13, 2022 (156)
119	14KJPN Submission ignored due to conflicting rows: Row 40168690 (NC_000005.10:17427297::TT 9355/28126) Row 40168691 (NC_000005.10:17427297::T 3065/28126) Row 40168692 (NC_000005.10:17427297:T: 1148/28126)...	-	Oct 13, 2022 (156)
120	UK 10K study - Twins Submission ignored due to conflicting rows: Row 14284851 (NC_000005.9:17427406::TTT 528/3708) Row 14284852 (NC_000005.9:17427406::T 1737/3708) Row 14284853 (NC_000005.9:17427406::TT 1399/3708)	-	Oct 12, 2018 (152)
121	UK 10K study - Twins Submission ignored due to conflicting rows: Row 14284851 (NC_000005.9:17427406::TTT 528/3708) Row 14284852 (NC_000005.9:17427406::T 1737/3708) Row 14284853 (NC_000005.9:17427406::TT 1399/3708)	-	Oct 12, 2018 (152)
122	UK 10K study - Twins Submission ignored due to conflicting rows: Row 14284851 (NC_000005.9:17427406::TTT 528/3708) Row 14284852 (NC_000005.9:17427406::T 1737/3708) Row 14284853 (NC_000005.9:17427406::TT 1399/3708)	-	Oct 12, 2018 (152)
123	ALFA	NC_000005.10 - 17427298	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).

Associated ID	History Updated (Build)
rs71601744	May 11, 2012 (137)
rs70943900	Oct 12, 2011 (135)
rs60142758	May 11, 2012 (137)
rs67022593	May 11, 2012 (137)
rs67022594	Feb 26, 2009 (130)
rs72072374	May 11, 2012 (137)
rs150794861	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4100112289	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4100112288	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4100112287	NC_000005.10:17427297:TTTTTTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4100112286, ss5263049131, ss5461380165, ss5893194105	NC_000005.10:17427297:TTTTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4100112285	NC_000005.10:17427297:TTTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4100112284	NC_000005.10:17427297:TTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4100112283	NC_000005.10:17427297:TTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4100112282	NC_000005.10:17427297:TTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4100112281, ss5706331590	NC_000005.10:17427297:TTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4100112280	NC_000005.10:17427297:TTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112279	NC_000005.10:17427297:TTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss2996515010	NC_000005.9:17427406:TT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3956183691, ss4100112278, ss5263049128, ss5461380164	NC_000005.10:17427297:TT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295214708	NC_000005.8:17480430:T:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5170597034	NC_000005.9:17427406:T:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5461380163, ss5706331588	NC_000005.10:17427297:T:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3956183687	NC_000005.10:17427298:T:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss98672875	NT_006576.16:17417406:T:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95387489	NT_006576.16:17417430:T:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295214707	NC_000005.8:17480407::T	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1704581324, ss1704581348, ss3829119908, ss5170597033	NC_000005.9:17427406::T	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112261, ss5263049129, ss5461380161, ss5706331587	NC_000005.10:17427297::T	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3956183689	NC_000005.10:17427299::T	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1704581326, ss1704581351, ss5170597032, ss5834587531	NC_000005.9:17427406::TT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112262, ss5461380162, ss5706331586	NC_000005.10:17427297::TT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3956183688	NC_000005.10:17427299::TT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss98672875	NT_006576.16:17417406:T:TTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss82000434	NT_006576.16:17417431::TT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1704581323, ss1704581345, ss5170597035, ss5834587532	NC_000005.9:17427406::TTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112263, ss5263049130, ss5706331589	NC_000005.10:17427297::TTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3956183690	NC_000005.10:17427299::TTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5170597036	NC_000005.9:17427406::TTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112264, ss5706331591	NC_000005.10:17427297::TTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3956183692	NC_000005.10:17427299::TTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112265	NC_000005.10:17427297::TTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112266	NC_000005.10:17427297::TTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112267	NC_000005.10:17427297::TTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112268	NC_000005.10:17427297::TTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112269	NC_000005.10:17427297::TTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112270	NC_000005.10:17427297::TTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112271	NC_000005.10:17427297::TTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112272	NC_000005.10:17427297::TTTTTTTTTTT… NC_000005.10:17427297::TTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112273	NC_000005.10:17427297::TTTTTTTTTTT… NC_000005.10:17427297::TTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112274	NC_000005.10:17427297::TTTTTTTTTTT… NC_000005.10:17427297::TTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112275	NC_000005.10:17427297::TTTTTTTTTTT… NC_000005.10:17427297::TTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4100112276	NC_000005.10:17427297::TTTTTTTTTTT… NC_000005.10:17427297::TTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5501266316	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2439772650	NC_000005.9:17427406:TTTTTTTT:	NC_000005.10:17427297:TTTTTTTTTTTT… NC_000005.10:17427297:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

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

No publications for rs34389091

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

rs34389091