Name: rs57700679
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.

rs57700679

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:207593085-207593103 (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(A)₇ / del(A)₆ / del(A)₅ / del(…
del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₂ / dup(A)₁₃ / dup(A)₁₄ / dup(A)₁₅ / dup(A)₁₆ / dup(A)₁₇ / dup(A)₁₈ / dup(A)₁₉ / ins(A)₂₀ / ins(A)₂₄ / ins(A)₅(TTAAAA)₂AAAAAAAAAAAAAAAAAAA
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₇=0.0000 (0/6210, ALFA)
del(A)₆=0.0000 (0/6210, ALFA)
del(A)₅=0.0000 (0/6210, ALFA) (+ 15 more)
del(A)₄=0.0000 (0/6210, ALFA)
delAAA=0.0000 (0/6210, ALFA)
delAA=0.0000 (0/6210, ALFA)
delA=0.0000 (0/6210, ALFA)
dupA=0.0000 (0/6210, ALFA)
dupAA=0.0000 (0/6210, ALFA)
dupAAA=0.0000 (0/6210, ALFA)
dup(A)₄=0.0000 (0/6210, ALFA)
dup(A)₅=0.0000 (0/6210, ALFA)
dup(A)₆=0.0000 (0/6210, ALFA)
dup(A)₇=0.0000 (0/6210, ALFA)
dup(A)₈=0.0000 (0/6210, ALFA)
dup(A)₉=0.0000 (0/6210, ALFA)
dup(A)₁₀=0.0000 (0/6210, ALFA)
dup(A)₁₁=0.0000 (0/6210, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CR1 : 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	6210	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	5096	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African	Sub	486	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	14	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	472	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	10	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	80	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	302	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	34	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	202	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6210	(A)₁₉=1.0000	del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000, dup(A)₇=0.0000, dup(A)₈=0.0000, dup(A)₉=0.0000, dup(A)₁₀=0.0000, dup(A)₁₁=0.0000
Allele Frequency Aggregator	European	Sub	5096	(A)₁₉=1.0000	del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000, dup(A)₇=0.0000, dup(A)₈=0.0000, dup(A)₉=0.0000, dup(A)₁₀=0.0000, dup(A)₁₁=0.0000
Allele Frequency Aggregator	African	Sub	486	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₈=0.000, dup(A)₉=0.000, dup(A)₁₀=0.000, dup(A)₁₁=0.000
Allele Frequency Aggregator	Latin American 2	Sub	302	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₈=0.000, dup(A)₉=0.000, dup(A)₁₀=0.000, dup(A)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	202	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₈=0.000, dup(A)₉=0.000, dup(A)₁₀=0.000, dup(A)₁₁=0.000
Allele Frequency Aggregator	Latin American 1	Sub	80	(A)₁₉=1.00	del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00, dup(A)₁₀=0.00, dup(A)₁₁=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(A)₁₉=1.00	del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00, dup(A)₁₀=0.00, dup(A)₁₁=0.00
Allele Frequency Aggregator	Asian	Sub	10	(A)₁₉=1.0	del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0, dup(A)₆=0.0, dup(A)₇=0.0, dup(A)₈=0.0, dup(A)₉=0.0, dup(A)₁₀=0.0, dup(A)₁₁=0.0

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 1	NC_000001.11:g.207593097_207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593098_207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593099_207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593100_207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593101_207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593102_207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593103del
GRCh38.p14 chr 1	NC_000001.11:g.207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593102_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593101_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593100_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593099_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593098_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593097_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593096_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593095_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593094_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593093_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593092_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593091_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593090_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593089_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593088_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593087_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593086_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593085_207593103dup
GRCh38.p14 chr 1	NC_000001.11:g.207593103_207593104insAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 1	NC_000001.11:g.207593103_207593104insAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 1	NC_000001.11:g.207593085_207593103A[24]TTAAAA[2]A[19]
GRCh37.p13 chr 1	NC_000001.10:g.207766442_207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766443_207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766444_207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766445_207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766446_207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766447_207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766448del
GRCh37.p13 chr 1	NC_000001.10:g.207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766447_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766446_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766445_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766444_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766443_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766442_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766441_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766440_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766439_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766438_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766437_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766436_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766435_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766434_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766433_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766432_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766431_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766430_207766448dup
GRCh37.p13 chr 1	NC_000001.10:g.207766448_207766449insAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.207766448_207766449insAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.207766430_207766448A[24]TTAAAA[2]A[19]
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101970_101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101971_101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101972_101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101973_101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101974_101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101975_101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101976del
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101975_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101974_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101973_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101972_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101971_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101970_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101969_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101968_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101967_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101966_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101965_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101964_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101963_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101962_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101961_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101960_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101959_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101958_101976dup
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101976_101977insAAAAAAAAAAAAAAAAAAAA
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101976_101977insAAAAAAAAAAAAAAAAAAAAAAAA
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101958_101976A[24]TTAAAA[2]A[19]

Gene: CR1, complement C3b/C4b receptor 1 (Knops blood group) (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CR1 transcript variant S	NM_000651.6:c.5810+4323_5… NM_000651.6:c.5810+4323_5810+4329del	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	(A)₁₉=	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₂	dup(A)₁₃	dup(A)₁₄	dup(A)₁₅	dup(A)₁₆	dup(A)₁₇	dup(A)₁₈	dup(A)₁₉	ins(A)₂₀	ins(A)₂₄	ins(A)₅(TTAAAA)₂AAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 1	NC_000001.11:g.207593085_207593103=	NC_000001.11:g.207593097_207593103del	NC_000001.11:g.207593098_207593103del	NC_000001.11:g.207593099_207593103del	NC_000001.11:g.207593100_207593103del	NC_000001.11:g.207593101_207593103del	NC_000001.11:g.207593102_207593103del	NC_000001.11:g.207593103del	NC_000001.11:g.207593103dup	NC_000001.11:g.207593102_207593103dup	NC_000001.11:g.207593101_207593103dup	NC_000001.11:g.207593100_207593103dup	NC_000001.11:g.207593099_207593103dup	NC_000001.11:g.207593098_207593103dup	NC_000001.11:g.207593097_207593103dup	NC_000001.11:g.207593096_207593103dup	NC_000001.11:g.207593095_207593103dup	NC_000001.11:g.207593094_207593103dup	NC_000001.11:g.207593093_207593103dup	NC_000001.11:g.207593092_207593103dup	NC_000001.11:g.207593091_207593103dup	NC_000001.11:g.207593090_207593103dup	NC_000001.11:g.207593089_207593103dup	NC_000001.11:g.207593088_207593103dup	NC_000001.11:g.207593087_207593103dup	NC_000001.11:g.207593086_207593103dup	NC_000001.11:g.207593085_207593103dup	NC_000001.11:g.207593103_207593104insAAAAAAAAAAAAAAAAAAAA	NC_000001.11:g.207593103_207593104insAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:g.207593085_207593103A[24]TTAAAA[2]A[19]
GRCh37.p13 chr 1	NC_000001.10:g.207766430_207766448=	NC_000001.10:g.207766442_207766448del	NC_000001.10:g.207766443_207766448del	NC_000001.10:g.207766444_207766448del	NC_000001.10:g.207766445_207766448del	NC_000001.10:g.207766446_207766448del	NC_000001.10:g.207766447_207766448del	NC_000001.10:g.207766448del	NC_000001.10:g.207766448dup	NC_000001.10:g.207766447_207766448dup	NC_000001.10:g.207766446_207766448dup	NC_000001.10:g.207766445_207766448dup	NC_000001.10:g.207766444_207766448dup	NC_000001.10:g.207766443_207766448dup	NC_000001.10:g.207766442_207766448dup	NC_000001.10:g.207766441_207766448dup	NC_000001.10:g.207766440_207766448dup	NC_000001.10:g.207766439_207766448dup	NC_000001.10:g.207766438_207766448dup	NC_000001.10:g.207766437_207766448dup	NC_000001.10:g.207766436_207766448dup	NC_000001.10:g.207766435_207766448dup	NC_000001.10:g.207766434_207766448dup	NC_000001.10:g.207766433_207766448dup	NC_000001.10:g.207766432_207766448dup	NC_000001.10:g.207766431_207766448dup	NC_000001.10:g.207766430_207766448dup	NC_000001.10:g.207766448_207766449insAAAAAAAAAAAAAAAAAAAA	NC_000001.10:g.207766448_207766449insAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.10:g.207766430_207766448A[24]TTAAAA[2]A[19]
Knops blood group RefSeqGene (LRG_814)	NG_007481.1:g.101958_101976=	NG_007481.1:g.101970_101976del	NG_007481.1:g.101971_101976del	NG_007481.1:g.101972_101976del	NG_007481.1:g.101973_101976del	NG_007481.1:g.101974_101976del	NG_007481.1:g.101975_101976del	NG_007481.1:g.101976del	NG_007481.1:g.101976dup	NG_007481.1:g.101975_101976dup	NG_007481.1:g.101974_101976dup	NG_007481.1:g.101973_101976dup	NG_007481.1:g.101972_101976dup	NG_007481.1:g.101971_101976dup	NG_007481.1:g.101970_101976dup	NG_007481.1:g.101969_101976dup	NG_007481.1:g.101968_101976dup	NG_007481.1:g.101967_101976dup	NG_007481.1:g.101966_101976dup	NG_007481.1:g.101965_101976dup	NG_007481.1:g.101964_101976dup	NG_007481.1:g.101963_101976dup	NG_007481.1:g.101962_101976dup	NG_007481.1:g.101961_101976dup	NG_007481.1:g.101960_101976dup	NG_007481.1:g.101959_101976dup	NG_007481.1:g.101958_101976dup	NG_007481.1:g.101976_101977insAAAAAAAAAAAAAAAAAAAA	NG_007481.1:g.101976_101977insAAAAAAAAAAAAAAAAAAAAAAAA	NG_007481.1:g.101958_101976A[24]TTAAAA[2]A[19]
CR1 transcript variant F	NM_000573.3:c.4460+4311=	NM_000573.3:c.4460+4323_4460+4329del	NM_000573.3:c.4460+4324_4460+4329del	NM_000573.3:c.4460+4325_4460+4329del	NM_000573.3:c.4460+4326_4460+4329del	NM_000573.3:c.4460+4327_4460+4329del	NM_000573.3:c.4460+4328_4460+4329del	NM_000573.3:c.4460+4329del	NM_000573.3:c.4460+4329dup	NM_000573.3:c.4460+4328_4460+4329dup	NM_000573.3:c.4460+4327_4460+4329dup	NM_000573.3:c.4460+4326_4460+4329dup	NM_000573.3:c.4460+4325_4460+4329dup	NM_000573.3:c.4460+4324_4460+4329dup	NM_000573.3:c.4460+4323_4460+4329dup	NM_000573.3:c.4460+4322_4460+4329dup	NM_000573.3:c.4460+4321_4460+4329dup	NM_000573.3:c.4460+4320_4460+4329dup	NM_000573.3:c.4460+4319_4460+4329dup	NM_000573.3:c.4460+4318_4460+4329dup	NM_000573.3:c.4460+4317_4460+4329dup	NM_000573.3:c.4460+4316_4460+4329dup	NM_000573.3:c.4460+4315_4460+4329dup	NM_000573.3:c.4460+4314_4460+4329dup	NM_000573.3:c.4460+4313_4460+4329dup	NM_000573.3:c.4460+4312_4460+4329dup	NM_000573.3:c.4460+4311_4460+4329dup	NM_000573.3:c.4460+4329_4460+4330insAAAAAAAAAAAAAAAAAAAA	NM_000573.3:c.4460+4329_4460+4330insAAAAAAAAAAAAAAAAAAAAAAAA	NM_000573.3:c.4460+4329_4460+4330insAAAAATTAAAATTAAAAAAAAAAAAAAAAAAAAAAA
CR1 transcript variant S	NM_000651.4:c.5810+4311=	NM_000651.4:c.5810+4323_5810+4329del	NM_000651.4:c.5810+4324_5810+4329del	NM_000651.4:c.5810+4325_5810+4329del	NM_000651.4:c.5810+4326_5810+4329del	NM_000651.4:c.5810+4327_5810+4329del	NM_000651.4:c.5810+4328_5810+4329del	NM_000651.4:c.5810+4329del	NM_000651.4:c.5810+4329dup	NM_000651.4:c.5810+4328_5810+4329dup	NM_000651.4:c.5810+4327_5810+4329dup	NM_000651.4:c.5810+4326_5810+4329dup	NM_000651.4:c.5810+4325_5810+4329dup	NM_000651.4:c.5810+4324_5810+4329dup	NM_000651.4:c.5810+4323_5810+4329dup	NM_000651.4:c.5810+4322_5810+4329dup	NM_000651.4:c.5810+4321_5810+4329dup	NM_000651.4:c.5810+4320_5810+4329dup	NM_000651.4:c.5810+4319_5810+4329dup	NM_000651.4:c.5810+4318_5810+4329dup	NM_000651.4:c.5810+4317_5810+4329dup	NM_000651.4:c.5810+4316_5810+4329dup	NM_000651.4:c.5810+4315_5810+4329dup	NM_000651.4:c.5810+4314_5810+4329dup	NM_000651.4:c.5810+4313_5810+4329dup	NM_000651.4:c.5810+4312_5810+4329dup	NM_000651.4:c.5810+4311_5810+4329dup	NM_000651.4:c.5810+4329_5810+4330insAAAAAAAAAAAAAAAAAAAA	NM_000651.4:c.5810+4329_5810+4330insAAAAAAAAAAAAAAAAAAAAAAAA	NM_000651.4:c.5810+4329_5810+4330insAAAAATTAAAATTAAAAAAAAAAAAAAAAAAAAAAA
CR1 transcript variant S	NM_000651.6:c.5810+4311=	NM_000651.6:c.5810+4323_5810+4329del	NM_000651.6:c.5810+4324_5810+4329del	NM_000651.6:c.5810+4325_5810+4329del	NM_000651.6:c.5810+4326_5810+4329del	NM_000651.6:c.5810+4327_5810+4329del	NM_000651.6:c.5810+4328_5810+4329del	NM_000651.6:c.5810+4329del	NM_000651.6:c.5810+4329dup	NM_000651.6:c.5810+4328_5810+4329dup	NM_000651.6:c.5810+4327_5810+4329dup	NM_000651.6:c.5810+4326_5810+4329dup	NM_000651.6:c.5810+4325_5810+4329dup	NM_000651.6:c.5810+4324_5810+4329dup	NM_000651.6:c.5810+4323_5810+4329dup	NM_000651.6:c.5810+4322_5810+4329dup	NM_000651.6:c.5810+4321_5810+4329dup	NM_000651.6:c.5810+4320_5810+4329dup	NM_000651.6:c.5810+4319_5810+4329dup	NM_000651.6:c.5810+4318_5810+4329dup	NM_000651.6:c.5810+4317_5810+4329dup	NM_000651.6:c.5810+4316_5810+4329dup	NM_000651.6:c.5810+4315_5810+4329dup	NM_000651.6:c.5810+4314_5810+4329dup	NM_000651.6:c.5810+4313_5810+4329dup	NM_000651.6:c.5810+4312_5810+4329dup	NM_000651.6:c.5810+4311_5810+4329dup	NM_000651.6:c.5810+4329_5810+4330insAAAAAAAAAAAAAAAAAAAA	NM_000651.6:c.5810+4329_5810+4330insAAAAAAAAAAAAAAAAAAAAAAAA	NM_000651.6:c.5810+4329_5810+4330insAAAAATTAAAATTAAAAAAAAAAAAAAAAAAAAAAA
CR1 transcript variant X1	XM_005273064.1:c.5426+4311=	XM_005273064.1:c.5426+4323_5426+4329del	XM_005273064.1:c.5426+4324_5426+4329del	XM_005273064.1:c.5426+4325_5426+4329del	XM_005273064.1:c.5426+4326_5426+4329del	XM_005273064.1:c.5426+4327_5426+4329del	XM_005273064.1:c.5426+4328_5426+4329del	XM_005273064.1:c.5426+4329del	XM_005273064.1:c.5426+4329dup	XM_005273064.1:c.5426+4328_5426+4329dup	XM_005273064.1:c.5426+4327_5426+4329dup	XM_005273064.1:c.5426+4326_5426+4329dup	XM_005273064.1:c.5426+4325_5426+4329dup	XM_005273064.1:c.5426+4324_5426+4329dup	XM_005273064.1:c.5426+4323_5426+4329dup	XM_005273064.1:c.5426+4322_5426+4329dup	XM_005273064.1:c.5426+4321_5426+4329dup	XM_005273064.1:c.5426+4320_5426+4329dup	XM_005273064.1:c.5426+4319_5426+4329dup	XM_005273064.1:c.5426+4318_5426+4329dup	XM_005273064.1:c.5426+4317_5426+4329dup	XM_005273064.1:c.5426+4316_5426+4329dup	XM_005273064.1:c.5426+4315_5426+4329dup	XM_005273064.1:c.5426+4314_5426+4329dup	XM_005273064.1:c.5426+4313_5426+4329dup	XM_005273064.1:c.5426+4312_5426+4329dup	XM_005273064.1:c.5426+4311_5426+4329dup	XM_005273064.1:c.5426+4329_5426+4330insAAAAAAAAAAAAAAAAAAAA	XM_005273064.1:c.5426+4329_5426+4330insAAAAAAAAAAAAAAAAAAAAAAAA	XM_005273064.1:c.5426+4329_5426+4330insAAAAATTAAAATTAAAAAAAAAAAAAAAAAAAAAAA

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#.

60 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80247644	Dec 14, 2007 (129)
2	HGSV	ss83632278	Dec 14, 2007 (129)
3	HGSV	ss83638335	Dec 14, 2007 (129)
4	GMI	ss288084357	May 04, 2012 (137)
5	PJP	ss294622329	May 09, 2011 (134)
6	EVA_DECODE	ss3688502889	Jul 12, 2019 (153)
7	EVA_DECODE	ss3688502890	Jul 12, 2019 (153)
8	EVA_DECODE	ss3688502891	Jul 12, 2019 (153)
9	EVA_DECODE	ss3688502892	Jul 12, 2019 (153)
10	EVA_DECODE	ss3688502893	Jul 12, 2019 (153)
11	ACPOP	ss3727804818	Jul 12, 2019 (153)
12	ACPOP	ss3727804819	Jul 12, 2019 (153)
13	ACPOP	ss3727804821	Jul 12, 2019 (153)
14	ACPOP	ss3727804822	Jul 12, 2019 (153)
15	PACBIO	ss3789285674	Jul 12, 2019 (153)
16	PACBIO	ss3794157939	Jul 12, 2019 (153)
17	EVA	ss3826610047	Apr 25, 2020 (154)
18	GNOMAD	ss4010198960	Apr 25, 2021 (155)
19	GNOMAD	ss4010198961	Apr 25, 2021 (155)
20	GNOMAD	ss4010198962	Apr 25, 2021 (155)
21	GNOMAD	ss4010198963	Apr 25, 2021 (155)
22	GNOMAD	ss4010198964	Apr 25, 2021 (155)
23	GNOMAD	ss4010198965	Apr 25, 2021 (155)
24	GNOMAD	ss4010198966	Apr 25, 2021 (155)
25	GNOMAD	ss4010198967	Apr 25, 2021 (155)
26	GNOMAD	ss4010198968	Apr 25, 2021 (155)
27	GNOMAD	ss4010198969	Apr 25, 2021 (155)
28	GNOMAD	ss4010198970	Apr 25, 2021 (155)
29	GNOMAD	ss4010198971	Apr 25, 2021 (155)
30	GNOMAD	ss4010198972	Apr 25, 2021 (155)
31	GNOMAD	ss4010198973	Apr 25, 2021 (155)
32	GNOMAD	ss4010198974	Apr 25, 2021 (155)
33	GNOMAD	ss4010198975	Apr 25, 2021 (155)
34	GNOMAD	ss4010198976	Apr 25, 2021 (155)
35	GNOMAD	ss4010198977	Apr 25, 2021 (155)
36	GNOMAD	ss4010198978	Apr 25, 2021 (155)
37	GNOMAD	ss4010198979	Apr 25, 2021 (155)
38	GNOMAD	ss4010198980	Apr 25, 2021 (155)
39	GNOMAD	ss4010198981	Apr 25, 2021 (155)
40	GNOMAD	ss4010198982	Apr 25, 2021 (155)
41	GNOMAD	ss4010198983	Apr 25, 2021 (155)
42	GNOMAD	ss4010198984	Apr 25, 2021 (155)
43	GNOMAD	ss4010198985	Apr 25, 2021 (155)
44	GNOMAD	ss4010198986	Apr 25, 2021 (155)
45	TOMMO_GENOMICS	ss5148144249	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5148144250	Apr 25, 2021 (155)
47	TOMMO_GENOMICS	ss5148144251	Apr 25, 2021 (155)
48	TOMMO_GENOMICS	ss5148144252	Apr 25, 2021 (155)
49	TOMMO_GENOMICS	ss5148144253	Apr 25, 2021 (155)
50	HUGCELL_USP	ss5446031326	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5446031328	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5446031329	Oct 12, 2022 (156)
53	HUGCELL_USP	ss5446031330	Oct 12, 2022 (156)
54	HUGCELL_USP	ss5446031331	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5675823539	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5675823540	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5675823541	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5675823543	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5675823544	Oct 12, 2022 (156)
60	EVA	ss5849256423	Oct 12, 2022 (156)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37733664 (NC_000001.11:207593084::A 5926/76220) Row 37733665 (NC_000001.11:207593084::AA 1029/76272) Row 37733666 (NC_000001.11:207593084::AAA 33/76308)...	-	Apr 25, 2021 (155)
88	Northern Sweden Submission ignored due to conflicting rows: Row 1089683 (NC_000001.10:207766429::AAAAA 55/562) Row 1089684 (NC_000001.10:207766429::AAAAAAAA 13/562) Row 1089686 (NC_000001.10:207766429::A 11/562)...	-	Jul 12, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 1089683 (NC_000001.10:207766429::AAAAA 55/562) Row 1089684 (NC_000001.10:207766429::AAAAAAAA 13/562) Row 1089686 (NC_000001.10:207766429::A 11/562)...	-	Jul 12, 2019 (153)
90	Northern Sweden Submission ignored due to conflicting rows: Row 1089683 (NC_000001.10:207766429::AAAAA 55/562) Row 1089684 (NC_000001.10:207766429::AAAAAAAA 13/562) Row 1089686 (NC_000001.10:207766429::A 11/562)...	-	Jul 12, 2019 (153)
91	Northern Sweden Submission ignored due to conflicting rows: Row 1089683 (NC_000001.10:207766429::AAAAA 55/562) Row 1089684 (NC_000001.10:207766429::AAAAAAAA 13/562) Row 1089686 (NC_000001.10:207766429::A 11/562)...	-	Jul 12, 2019 (153)
92	8.3KJPN Submission ignored due to conflicting rows: Row 6113556 (NC_000001.10:207766429::AA 3967/16128) Row 6113557 (NC_000001.10:207766429:AAAAAAA: 404/16128) Row 6113558 (NC_000001.10:207766429::A 1037/16128)...	-	Apr 25, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 6113556 (NC_000001.10:207766429::AA 3967/16128) Row 6113557 (NC_000001.10:207766429:AAAAAAA: 404/16128) Row 6113558 (NC_000001.10:207766429::A 1037/16128)...	-	Apr 25, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 6113556 (NC_000001.10:207766429::AA 3967/16128) Row 6113557 (NC_000001.10:207766429:AAAAAAA: 404/16128) Row 6113558 (NC_000001.10:207766429::A 1037/16128)...	-	Apr 25, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 6113556 (NC_000001.10:207766429::AA 3967/16128) Row 6113557 (NC_000001.10:207766429:AAAAAAA: 404/16128) Row 6113558 (NC_000001.10:207766429::A 1037/16128)...	-	Apr 25, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 6113556 (NC_000001.10:207766429::AA 3967/16128) Row 6113557 (NC_000001.10:207766429:AAAAAAA: 404/16128) Row 6113558 (NC_000001.10:207766429::A 1037/16128)...	-	Apr 25, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 9660643 (NC_000001.11:207593084::AA 5946/26912) Row 9660644 (NC_000001.11:207593084::A 1625/26912) Row 9660645 (NC_000001.11:207593084::AAAAA 3482/26912)...	-	Oct 12, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 9660643 (NC_000001.11:207593084::AA 5946/26912) Row 9660644 (NC_000001.11:207593084::A 1625/26912) Row 9660645 (NC_000001.11:207593084::AAAAA 3482/26912)...	-	Oct 12, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 9660643 (NC_000001.11:207593084::AA 5946/26912) Row 9660644 (NC_000001.11:207593084::A 1625/26912) Row 9660645 (NC_000001.11:207593084::AAAAA 3482/26912)...	-	Oct 12, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 9660643 (NC_000001.11:207593084::AA 5946/26912) Row 9660644 (NC_000001.11:207593084::A 1625/26912) Row 9660645 (NC_000001.11:207593084::AAAAA 3482/26912)...	-	Oct 12, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 9660643 (NC_000001.11:207593084::AA 5946/26912) Row 9660644 (NC_000001.11:207593084::A 1625/26912) Row 9660645 (NC_000001.11:207593084::AAAAA 3482/26912)...	-	Oct 12, 2022 (156)
102	ALFA	NC_000001.11 - 207593085	Apr 25, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss288084357	NC_000001.9:205833052:AAAAAAA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5148144250	NC_000001.10:207766429:AAAAAAA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4010198986, ss5675823543	NC_000001.11:207593084:AAAAAAA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4010198985	NC_000001.11:207593084:AAAAAA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4010198984	NC_000001.11:207593084:AAAAA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4010198983	NC_000001.11:207593084:AAAA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4010198982	NC_000001.11:207593084:AA:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3688502893, ss4010198981, ss5446031330	NC_000001.11:207593084:A:	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3727804821, ss3789285674, ss3794157939, ss3826610047, ss5148144251	NC_000001.10:207766429::A	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4010198960, ss5446031328, ss5675823540	NC_000001.11:207593084::A	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3688502892	NC_000001.11:207593085::A	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5148144249	NC_000001.10:207766429::AA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198961, ss5675823539, ss5849256423	NC_000001.11:207593084::AA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198962	NC_000001.11:207593084::AAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198963	NC_000001.11:207593084::AAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3688502891	NC_000001.11:207593085::AAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294622329	NC_000001.9:205833053::AAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3727804818, ss5148144252	NC_000001.10:207766429::AAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198964, ss5446031326, ss5675823541	NC_000001.11:207593084::AAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3688502890	NC_000001.11:207593085::AAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5148144253	NC_000001.10:207766429::AAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198965, ss5446031329, ss5675823544	NC_000001.11:207593084::AAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3688502889	NC_000001.11:207593085::AAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss83632278, ss83638335	NT_167186.1:1284227::AAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198966	NC_000001.11:207593084::AAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80247644	NT_167186.1:1284227::AAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3727804819	NC_000001.10:207766429::AAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198967, ss5446031331	NC_000001.11:207593084::AAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198968	NC_000001.11:207593084::AAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198969	NC_000001.11:207593084::AAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198970	NC_000001.11:207593084::AAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2761100496	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198971	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198972	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198973	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198974	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198975	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198976	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198977	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198978	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198979	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3727804822	NC_000001.10:207766429::AAAAAAAAAA… NC_000001.10:207766429::AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4010198980	NC_000001.11:207593084::AAAAAAAAAA… NC_000001.11:207593084::AAAAAAAAAAAAAAAAAAAAAAAATTAAAATTAAAA	NC_000001.11:207593084:AAAAAAAAAAA… NC_000001.11:207593084:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAATTAAAATTAAAAAAAAAAAAAAAAAAAAAAA	(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 rs57700679

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

rs57700679