Name: rs71523910
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.

rs71523910

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:143405437-143405462 (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(GT)₈ / del(GT)₇ / del(GT)₆ / d…
del(GT)₈ / del(GT)₇ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupGT=0.2068 (1162/5618, ALFA)
delGTGT=0.3502 (1754/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: EPHA1 : 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	5618	GTGTGTGTGTGTGTGTGTGTGTGTGT=0.4970	GTGTGTGTGT=0.0000, GTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGT=0.1358, GTGTGTGTGTGTGTGTGTGTGTGT=0.0018, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.2068, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0061, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1508, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0018, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.609589	0.120548	0.269863	32
European	Sub	5058	GTGTGTGTGTGTGTGTGTGTGTGTGT=0.4427	GTGTGTGTGT=0.0000, GTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGT=0.1503, GTGTGTGTGTGTGTGTGTGTGTGT=0.0020, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.2291, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0067, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1673, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0020, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.518581	0.148649	0.33277	33
African	Sub	484	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGT=0.000, GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGT=0.00, GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	460	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGT=0.000, GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGT=0.0, GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGT=0.0, GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	GTGTGTGTGTGTGTGTGTGTGTGTGT=0	GTGTGTGTGT=0, GTGTGTGTGTGT=0, GTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 1	Sub	16	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGT=0.00, GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGT=0.00, GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	GTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGT=0.0, GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other	Sub	42	GTGTGTGTGTGTGTGTGTGTGTGTGT=0.83	GTGTGTGTGT=0.00, GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.07, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.07, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.02, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5618	(GT)₁₃=0.4970	del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.1358, delGT=0.0018, dupGT=0.2068, dupGTGT=0.0061, dup(GT)₃=0.1508, dup(GT)₄=0.0018, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000
Allele Frequency Aggregator	European	Sub	5058	(GT)₁₃=0.4427	del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.1503, delGT=0.0020, dupGT=0.2291, dupGTGT=0.0067, dup(GT)₃=0.1673, dup(GT)₄=0.0020, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000
Allele Frequency Aggregator	African	Sub	484	(GT)₁₃=1.000	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000
Allele Frequency Aggregator	Other	Sub	42	(GT)₁₃=0.83	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.07, delGT=0.00, dupGT=0.07, dupGTGT=0.00, dup(GT)₃=0.02, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(GT)₁₃=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00
Allele Frequency Aggregator	Latin American 2	Sub	14	(GT)₁₃=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	2	(GT)₁₃=1.0	del(GT)₈=0.0, del(GT)₇=0.0, del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0, dup(GT)₇=0.0, dup(GT)₈=0.0, dup(GT)₉=0.0
Allele Frequency Aggregator	Asian	Sub	2	(GT)₁₃=1.0	del(GT)₈=0.0, del(GT)₇=0.0, del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0, dup(GT)₇=0.0, dup(GT)₈=0.0, dup(GT)₉=0.0
1000Genomes	Global	Study-wide	5008	(GT)₁₃=0.6498	delGTGT=0.3502
1000Genomes	African	Sub	1322	(GT)₁₃=0.8396	delGTGT=0.1604
1000Genomes	East Asian	Sub	1008	(GT)₁₃=0.2411	delGTGT=0.7589
1000Genomes	Europe	Sub	1006	(GT)₁₃=0.8141	delGTGT=0.1859
1000Genomes	South Asian	Sub	978	(GT)₁₃=0.726	delGTGT=0.274
1000Genomes	American	Sub	694	(GT)₁₃=0.536	delGTGT=0.464

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 7	NC_000007.14:g.143405437GT[5]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[6]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[7]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[8]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[9]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[10]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[11]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[12]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[14]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[15]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[16]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[17]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[18]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[19]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[20]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[21]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[22]
GRCh38.p14 chr 7	NC_000007.14:g.143405437GT[23]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[5]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[6]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[7]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[8]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[9]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[10]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[11]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[12]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[14]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[15]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[16]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[17]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[18]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[19]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[20]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[21]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[22]
GRCh37.p13 chr 7	NC_000007.13:g.143102530GT[23]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[5]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[6]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[7]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[8]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[9]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[10]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[11]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[12]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[14]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[15]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[16]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[17]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[18]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[19]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[20]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[21]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[22]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801GT[23]

Gene: EPHA1, EPH receptor A1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
EPHA1 transcript	NM_005232.5:c.150+2149AC[… NM_005232.5:c.150+2149AC[5]	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	(GT)₁₃=	del(GT)₈	del(GT)₇	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀
GRCh38.p14 chr 7	NC_000007.14:g.143405437_143405462=	NC_000007.14:g.143405437GT[5]	NC_000007.14:g.143405437GT[6]	NC_000007.14:g.143405437GT[7]	NC_000007.14:g.143405437GT[8]	NC_000007.14:g.143405437GT[9]	NC_000007.14:g.143405437GT[10]	NC_000007.14:g.143405437GT[11]	NC_000007.14:g.143405437GT[12]	NC_000007.14:g.143405437GT[14]	NC_000007.14:g.143405437GT[15]	NC_000007.14:g.143405437GT[16]	NC_000007.14:g.143405437GT[17]	NC_000007.14:g.143405437GT[18]	NC_000007.14:g.143405437GT[19]	NC_000007.14:g.143405437GT[20]	NC_000007.14:g.143405437GT[21]	NC_000007.14:g.143405437GT[22]	NC_000007.14:g.143405437GT[23]
GRCh37.p13 chr 7	NC_000007.13:g.143102530_143102555=	NC_000007.13:g.143102530GT[5]	NC_000007.13:g.143102530GT[6]	NC_000007.13:g.143102530GT[7]	NC_000007.13:g.143102530GT[8]	NC_000007.13:g.143102530GT[9]	NC_000007.13:g.143102530GT[10]	NC_000007.13:g.143102530GT[11]	NC_000007.13:g.143102530GT[12]	NC_000007.13:g.143102530GT[14]	NC_000007.13:g.143102530GT[15]	NC_000007.13:g.143102530GT[16]	NC_000007.13:g.143102530GT[17]	NC_000007.13:g.143102530GT[18]	NC_000007.13:g.143102530GT[19]	NC_000007.13:g.143102530GT[20]	NC_000007.13:g.143102530GT[21]	NC_000007.13:g.143102530GT[22]	NC_000007.13:g.143102530GT[23]
GRCh38.p14 chr 7 fix patch HG708_PATCH	NW_018654714.1:g.24801_24826=	NW_018654714.1:g.24801GT[5]	NW_018654714.1:g.24801GT[6]	NW_018654714.1:g.24801GT[7]	NW_018654714.1:g.24801GT[8]	NW_018654714.1:g.24801GT[9]	NW_018654714.1:g.24801GT[10]	NW_018654714.1:g.24801GT[11]	NW_018654714.1:g.24801GT[12]	NW_018654714.1:g.24801GT[14]	NW_018654714.1:g.24801GT[15]	NW_018654714.1:g.24801GT[16]	NW_018654714.1:g.24801GT[17]	NW_018654714.1:g.24801GT[18]	NW_018654714.1:g.24801GT[19]	NW_018654714.1:g.24801GT[20]	NW_018654714.1:g.24801GT[21]	NW_018654714.1:g.24801GT[22]	NW_018654714.1:g.24801GT[23]
EPHA1 transcript	NM_005232.4:c.150+2174=	NM_005232.4:c.150+2149AC[5]	NM_005232.4:c.150+2149AC[6]	NM_005232.4:c.150+2149AC[7]	NM_005232.4:c.150+2149AC[8]	NM_005232.4:c.150+2149AC[9]	NM_005232.4:c.150+2149AC[10]	NM_005232.4:c.150+2149AC[11]	NM_005232.4:c.150+2149AC[12]	NM_005232.4:c.150+2149AC[14]	NM_005232.4:c.150+2149AC[15]	NM_005232.4:c.150+2149AC[16]	NM_005232.4:c.150+2149AC[17]	NM_005232.4:c.150+2149AC[18]	NM_005232.4:c.150+2149AC[19]	NM_005232.4:c.150+2149AC[20]	NM_005232.4:c.150+2149AC[21]	NM_005232.4:c.150+2149AC[22]	NM_005232.4:c.150+2149AC[23]
EPHA1 transcript	NM_005232.5:c.150+2174=	NM_005232.5:c.150+2149AC[5]	NM_005232.5:c.150+2149AC[6]	NM_005232.5:c.150+2149AC[7]	NM_005232.5:c.150+2149AC[8]	NM_005232.5:c.150+2149AC[9]	NM_005232.5:c.150+2149AC[10]	NM_005232.5:c.150+2149AC[11]	NM_005232.5:c.150+2149AC[12]	NM_005232.5:c.150+2149AC[14]	NM_005232.5:c.150+2149AC[15]	NM_005232.5:c.150+2149AC[16]	NM_005232.5:c.150+2149AC[17]	NM_005232.5:c.150+2149AC[18]	NM_005232.5:c.150+2149AC[19]	NM_005232.5:c.150+2149AC[20]	NM_005232.5:c.150+2149AC[21]	NM_005232.5:c.150+2149AC[22]	NM_005232.5:c.150+2149AC[23]

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#.

78 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss98215139	Feb 13, 2009 (130)
2	BUSHMAN	ss193951250	Jul 04, 2010 (136)
3	GMI	ss288878068	May 04, 2012 (137)
4	1000GENOMES	ss326998811	May 09, 2011 (134)
5	1000GENOMES	ss327056414	May 09, 2011 (135)
6	1000GENOMES	ss327364231	May 09, 2011 (135)
7	LUNTER	ss551796343	Apr 25, 2013 (138)
8	LUNTER	ss552007143	Apr 25, 2013 (138)
9	LUNTER	ss553321535	Apr 25, 2013 (138)
10	SSMP	ss663753163	Apr 01, 2015 (144)
11	BILGI_BIOE	ss666420159	Apr 25, 2013 (138)
12	1000GENOMES	ss1367768447	Aug 21, 2014 (142)
13	DDI	ss1536567506	Apr 01, 2015 (144)
14	SWEGEN	ss3002202987	Nov 08, 2017 (151)
15	MCHAISSO	ss3064278821	Nov 08, 2017 (151)
16	MCHAISSO	ss3065163125	Nov 08, 2017 (151)
17	MCHAISSO	ss3065163126	Nov 08, 2017 (151)
18	MCHAISSO	ss3066175253	Jan 10, 2018 (151)
19	MCHAISSO	ss3066175254	Nov 08, 2017 (151)
20	MCHAISSO	ss3066175255	Nov 08, 2017 (151)
21	URBANLAB	ss3648775423	Oct 12, 2018 (152)
22	EVA_DECODE	ss3720887806	Jul 13, 2019 (153)
23	PACBIO	ss3785985876	Jul 13, 2019 (153)
24	PACBIO	ss3791259838	Jul 13, 2019 (153)
25	PACBIO	ss3796140077	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3810442970	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3810442971	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3810442972	Jul 13, 2019 (153)
29	EVA	ss3830869976	Apr 26, 2020 (154)
30	KOGIC	ss3962769566	Apr 26, 2020 (154)
31	KOGIC	ss3962769567	Apr 26, 2020 (154)
32	KOGIC	ss3962769568	Apr 26, 2020 (154)
33	KOGIC	ss3962769569	Apr 26, 2020 (154)
34	KOGIC	ss3962769570	Apr 26, 2020 (154)
35	KOGIC	ss3962769571	Apr 26, 2020 (154)
36	GNOMAD	ss4174865713	Apr 26, 2021 (155)
37	GNOMAD	ss4174865716	Apr 26, 2021 (155)
38	GNOMAD	ss4174865717	Apr 26, 2021 (155)
39	GNOMAD	ss4174865719	Apr 26, 2021 (155)
40	GNOMAD	ss4174865720	Apr 26, 2021 (155)
41	GNOMAD	ss4174865721	Apr 26, 2021 (155)
42	GNOMAD	ss4174865722	Apr 26, 2021 (155)
43	GNOMAD	ss4174865723	Apr 26, 2021 (155)
44	GNOMAD	ss4174865724	Apr 26, 2021 (155)
45	GNOMAD	ss4174865726	Apr 26, 2021 (155)
46	GNOMAD	ss4174865727	Apr 26, 2021 (155)
47	GNOMAD	ss4174865728	Apr 26, 2021 (155)
48	GNOMAD	ss4174865729	Apr 26, 2021 (155)
49	GNOMAD	ss4174865730	Apr 26, 2021 (155)
50	GNOMAD	ss4174865731	Apr 26, 2021 (155)
51	GNOMAD	ss4174865732	Apr 26, 2021 (155)
52	GNOMAD	ss4174865733	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5186031237	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5186031238	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5186031239	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5186031240	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5186031241	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5186031242	Apr 26, 2021 (155)
59	1000G_HIGH_COVERAGE	ss5275090231	Oct 13, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5275090232	Oct 13, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5275090233	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5275090234	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5275090235	Oct 13, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5275090236	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5471936705	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5471936706	Oct 13, 2022 (156)
67	HUGCELL_USP	ss5471936707	Oct 13, 2022 (156)
68	HUGCELL_USP	ss5471936708	Oct 13, 2022 (156)
69	HUGCELL_USP	ss5471936709	Oct 13, 2022 (156)
70	HUGCELL_USP	ss5471936710	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5727175825	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5727175826	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5727175827	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5727175828	Oct 13, 2022 (156)
75	TOMMO_GENOMICS	ss5727175829	Oct 13, 2022 (156)
76	TOMMO_GENOMICS	ss5727175830	Oct 13, 2022 (156)
77	EVA	ss5823659421	Oct 13, 2022 (156)
78	EVA	ss5823659422	Oct 13, 2022 (156)
79	1000Genomes	NC_000007.13 - 143102530	Oct 12, 2018 (152)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 279542126 (NC_000007.14:143405436::GT 38393/137566) Row 279542129 (NC_000007.14:143405436::GTGT 701/137604) Row 279542130 (NC_000007.14:143405436::GTGTGT 25129/137584)...	-	Apr 26, 2021 (155)
97	Korean Genome Project Submission ignored due to conflicting rows: Row 19147567 (NC_000007.14:143405436:GTGTGT: 102/1832) Row 19147568 (NC_000007.14:143405438:GTGT: 1184/1832) Row 19147569 (NC_000007.14:143405442::GTGTGT 250/1832)...	-	Apr 26, 2020 (154)
98	Korean Genome Project Submission ignored due to conflicting rows: Row 19147567 (NC_000007.14:143405436:GTGTGT: 102/1832) Row 19147568 (NC_000007.14:143405438:GTGT: 1184/1832) Row 19147569 (NC_000007.14:143405442::GTGTGT 250/1832)...	-	Apr 26, 2020 (154)
99	Korean Genome Project Submission ignored due to conflicting rows: Row 19147567 (NC_000007.14:143405436:GTGTGT: 102/1832) Row 19147568 (NC_000007.14:143405438:GTGT: 1184/1832) Row 19147569 (NC_000007.14:143405442::GTGTGT 250/1832)...	-	Apr 26, 2020 (154)
100	Korean Genome Project Submission ignored due to conflicting rows: Row 19147567 (NC_000007.14:143405436:GTGTGT: 102/1832) Row 19147568 (NC_000007.14:143405438:GTGT: 1184/1832) Row 19147569 (NC_000007.14:143405442::GTGTGT 250/1832)...	-	Apr 26, 2020 (154)
101	Korean Genome Project Submission ignored due to conflicting rows: Row 19147567 (NC_000007.14:143405436:GTGTGT: 102/1832) Row 19147568 (NC_000007.14:143405438:GTGT: 1184/1832) Row 19147569 (NC_000007.14:143405442::GTGTGT 250/1832)...	-	Apr 26, 2020 (154)
102	Korean Genome Project Submission ignored due to conflicting rows: Row 19147567 (NC_000007.14:143405436:GTGTGT: 102/1832) Row 19147568 (NC_000007.14:143405438:GTGT: 1184/1832) Row 19147569 (NC_000007.14:143405442::GTGTGT 250/1832)...	-	Apr 26, 2020 (154)
103	8.3KJPN Submission ignored due to conflicting rows: Row 44000544 (NC_000007.13:143102529:GTGT: 11334/16758) Row 44000545 (NC_000007.13:143102529::GTGTGT 2838/16758) Row 44000546 (NC_000007.13:143102529:GT: 317/16758)...	-	Apr 26, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 44000544 (NC_000007.13:143102529:GTGT: 11334/16758) Row 44000545 (NC_000007.13:143102529::GTGTGT 2838/16758) Row 44000546 (NC_000007.13:143102529:GT: 317/16758)...	-	Apr 26, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 44000544 (NC_000007.13:143102529:GTGT: 11334/16758) Row 44000545 (NC_000007.13:143102529::GTGTGT 2838/16758) Row 44000546 (NC_000007.13:143102529:GT: 317/16758)...	-	Apr 26, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 44000544 (NC_000007.13:143102529:GTGT: 11334/16758) Row 44000545 (NC_000007.13:143102529::GTGTGT 2838/16758) Row 44000546 (NC_000007.13:143102529:GT: 317/16758)...	-	Apr 26, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 44000544 (NC_000007.13:143102529:GTGT: 11334/16758) Row 44000545 (NC_000007.13:143102529::GTGTGT 2838/16758) Row 44000546 (NC_000007.13:143102529:GT: 317/16758)...	-	Apr 26, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 44000544 (NC_000007.13:143102529:GTGT: 11334/16758) Row 44000545 (NC_000007.13:143102529::GTGTGT 2838/16758) Row 44000546 (NC_000007.13:143102529:GT: 317/16758)...	-	Apr 26, 2021 (155)
109	14KJPN Submission ignored due to conflicting rows: Row 61012929 (NC_000007.14:143405436::GTGTGT 4453/28242) Row 61012930 (NC_000007.14:143405436::GT 637/28242) Row 61012931 (NC_000007.14:143405436:GTGT: 19293/28242)...	-	Oct 13, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 61012929 (NC_000007.14:143405436::GTGTGT 4453/28242) Row 61012930 (NC_000007.14:143405436::GT 637/28242) Row 61012931 (NC_000007.14:143405436:GTGT: 19293/28242)...	-	Oct 13, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 61012929 (NC_000007.14:143405436::GTGTGT 4453/28242) Row 61012930 (NC_000007.14:143405436::GT 637/28242) Row 61012931 (NC_000007.14:143405436:GTGT: 19293/28242)...	-	Oct 13, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 61012929 (NC_000007.14:143405436::GTGTGT 4453/28242) Row 61012930 (NC_000007.14:143405436::GT 637/28242) Row 61012931 (NC_000007.14:143405436:GTGT: 19293/28242)...	-	Oct 13, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 61012929 (NC_000007.14:143405436::GTGTGT 4453/28242) Row 61012930 (NC_000007.14:143405436::GT 637/28242) Row 61012931 (NC_000007.14:143405436:GTGT: 19293/28242)...	-	Oct 13, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 61012929 (NC_000007.14:143405436::GTGTGT 4453/28242) Row 61012930 (NC_000007.14:143405436::GT 637/28242) Row 61012931 (NC_000007.14:143405436:GTGT: 19293/28242)...	-	Oct 13, 2022 (156)
115	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 4904829 (NC_000007.13:143102529:GTGT: 141/168) Row 4904830 (NC_000007.13:143102529::GTGTGT 19/46) Row 4904831 (NC_000007.13:143102529::GT 11/38)	-	Jul 13, 2019 (153)
116	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 4904829 (NC_000007.13:143102529:GTGT: 141/168) Row 4904830 (NC_000007.13:143102529::GTGTGT 19/46) Row 4904831 (NC_000007.13:143102529::GT 11/38)	-	Jul 13, 2019 (153)
117	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 4904829 (NC_000007.13:143102529:GTGT: 141/168) Row 4904830 (NC_000007.13:143102529::GTGTGT 19/46) Row 4904831 (NC_000007.13:143102529::GT 11/38)	-	Jul 13, 2019 (153)
118	ALFA	NC_000007.14 - 143405437	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)
rs112886117	Oct 17, 2011 (136)
rs145099460	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4174865733	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGT	(self)
ss4174865732	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
ss4174865731	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
ss4174865730	NC_000007.14:143405436:GTGTGTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	(self)
ss4174865729	NC_000007.14:143405436:GTGTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
ss5186031241	NC_000007.13:143102529:GTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
ss3962769566, ss4174865728, ss5727175829	NC_000007.14:143405436:GTGTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
ss288878068, ss326998811	NC_000007.12:142812651:GTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
39585513, ss663753163, ss1367768447, ss1536567506, ss3002202987, ss3830869976, ss5186031237, ss5823659422	NC_000007.13:143102529:GTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss3066175254, ss3810442972, ss4174865727, ss5275090234, ss5471936707, ss5727175827	NC_000007.14:143405436:GTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss3962769567	NC_000007.14:143405438:GTGT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss5186031239	NC_000007.13:143102529:GT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3066175253, ss4174865726, ss5275090235, ss5471936705, ss5727175828	NC_000007.14:143405436:GT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3962769569	NC_000007.14:143405440:GT:	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss327056414, ss327364231, ss551796343	NC_000007.12:142812651::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss666420159, ss3785985876, ss3791259838, ss3796140077, ss5186031240, ss5823659421	NC_000007.13:143102529::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065163126, ss4174865713, ss5275090231, ss5471936708, ss5727175826	NC_000007.14:143405436::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3810442970	NC_000007.14:143405440::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3962769570	NC_000007.14:143405442::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3720887806	NC_000007.14:143405450::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3648775423	NC_000007.14:143405459::TG	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss98215139	NT_007914.15:3698152::GT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865716, ss5471936710	NC_000007.14:143405436::GTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss552007143, ss553321535	NC_000007.12:142812651::GTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5186031238	NC_000007.13:143102529::GTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064278821, ss3065163125, ss3066175255, ss4174865717, ss5275090232, ss5471936706, ss5727175825	NC_000007.14:143405436::GTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3810442971	NC_000007.14:143405440::GTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3962769568	NC_000007.14:143405442::GTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss193951250	NT_007933.16:80898657::GTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5186031242	NC_000007.13:143102529::GTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865719, ss5275090236, ss5727175830	NC_000007.14:143405436::GTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3962769571	NC_000007.14:143405442::GTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865720, ss5275090233, ss5471936709	NC_000007.14:143405436::GTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865721	NC_000007.14:143405436::GTGTGTGTGT… NC_000007.14:143405436::GTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865722	NC_000007.14:143405436::GTGTGTGTGT… NC_000007.14:143405436::GTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865723	NC_000007.14:143405436::GTGTGTGTGT… NC_000007.14:143405436::GTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4080511032	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4174865724	NC_000007.14:143405436::GTGTGTGTGT… NC_000007.14:143405436::GTGTGTGTGTGTGTGTGTGT	NC_000007.14:143405436:GTGTGTGTGTG… NC_000007.14:143405436:GTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs71523910

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71523910