Name: rs11413169
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.

rs11413169

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:41628966-41628989 (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)₁₄ / del(A)₁₂ / del(A)₁₁ / d…
del(A)₁₄ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / 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)₁₆ / dup(A)₂₃ / ins(A)₃₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.000034 (9/264690, TOPMED)
del(A)₁₄=0.0000 (0/1116, ALFA)
del(A)₁₂=0.0000 (0/1116, ALFA) (+ 15 more)
del(A)₁₁=0.0000 (0/1116, ALFA)
del(A)₁₀=0.0000 (0/1116, ALFA)
del(A)₉=0.0000 (0/1116, ALFA)
del(A)₈=0.0000 (0/1116, ALFA)
del(A)₇=0.0000 (0/1116, ALFA)
del(A)₆=0.0000 (0/1116, ALFA)
del(A)₅=0.0000 (0/1116, ALFA)
del(A)₄=0.0000 (0/1116, ALFA)
delAAA=0.0000 (0/1116, ALFA)
delAA=0.0000 (0/1116, ALFA)
delA=0.0000 (0/1116, ALFA)
dupA=0.0000 (0/1116, ALFA)
dupAA=0.0000 (0/1116, ALFA)
dupAAA=0.0000 (0/1116, ALFA)
dup(A)₆=0.0000 (0/1116, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: XRCC6 : 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	1116	AAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	568	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	232	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	230	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	216	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	12	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	56	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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
TopMed	Global	Study-wide	264690	(A)₂₄=0.999966	del(A)₁₁=0.000034
Allele Frequency Aggregator	Total	Global	1116	(A)₂₄=1.0000	del(A)₁₄=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, 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)₆=0.0000
Allele Frequency Aggregator	European	Sub	568	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, 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)₆=0.000
Allele Frequency Aggregator	African	Sub	232	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, 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)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	216	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, 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)₆=0.000
Allele Frequency Aggregator	Other	Sub	56	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, 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)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, 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)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, 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)₆=0.00
Allele Frequency Aggregator	Asian	Sub	10	(A)₂₄=1.0	del(A)₁₄=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, 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)₆=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 22	NC_000022.11:g.41628976_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628978_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628979_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628980_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628981_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628982_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628983_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628984_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628985_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628986_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628987_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628988_41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628989del
GRCh38.p14 chr 22	NC_000022.11:g.41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628988_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628987_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628986_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628985_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628984_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628983_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628982_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628981_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628974_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628967_41628989dup
GRCh38.p14 chr 22	NC_000022.11:g.41628989_41628990insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 22	NC_000022.10:g.42024980_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024982_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024983_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024984_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024985_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024986_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024987_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024988_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024989_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024990_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024991_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024992_42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024993del
GRCh37.p13 chr 22	NC_000022.10:g.42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024992_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024991_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024990_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024989_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024988_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024987_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024986_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024985_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024978_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024971_42024993dup
GRCh37.p13 chr 22	NC_000022.10:g.42024993_42024994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: XRCC6, X-ray repair cross complementing 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
XRCC6 transcript variant 2	NM_001288976.2:c.195+746_… NM_001288976.2:c.195+746_195+759del	N/A	Intron Variant
XRCC6 transcript variant 3	NM_001288977.2:c.195+746_… NM_001288977.2:c.195+746_195+759del	N/A	Intron Variant
XRCC6 transcript variant 4	NM_001288978.2:c.45+6890_… NM_001288978.2:c.45+6890_45+6903del	N/A	Intron Variant
XRCC6 transcript variant 1	NM_001469.5:c.195+746_195… NM_001469.5:c.195+746_195+759del	N/A	Intron Variant
XRCC6 transcript variant X1	XM_047441304.1:c.45+6890_… XM_047441304.1:c.45+6890_45+6903del	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)₂₄=	del(A)₁₄	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	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)₁₆	dup(A)₂₃	ins(A)₃₉
GRCh38.p14 chr 22	NC_000022.11:g.41628966_41628989=	NC_000022.11:g.41628976_41628989del	NC_000022.11:g.41628978_41628989del	NC_000022.11:g.41628979_41628989del	NC_000022.11:g.41628980_41628989del	NC_000022.11:g.41628981_41628989del	NC_000022.11:g.41628982_41628989del	NC_000022.11:g.41628983_41628989del	NC_000022.11:g.41628984_41628989del	NC_000022.11:g.41628985_41628989del	NC_000022.11:g.41628986_41628989del	NC_000022.11:g.41628987_41628989del	NC_000022.11:g.41628988_41628989del	NC_000022.11:g.41628989del	NC_000022.11:g.41628989dup	NC_000022.11:g.41628988_41628989dup	NC_000022.11:g.41628987_41628989dup	NC_000022.11:g.41628986_41628989dup	NC_000022.11:g.41628985_41628989dup	NC_000022.11:g.41628984_41628989dup	NC_000022.11:g.41628983_41628989dup	NC_000022.11:g.41628982_41628989dup	NC_000022.11:g.41628981_41628989dup	NC_000022.11:g.41628974_41628989dup	NC_000022.11:g.41628967_41628989dup	NC_000022.11:g.41628989_41628990insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 22	NC_000022.10:g.42024970_42024993=	NC_000022.10:g.42024980_42024993del	NC_000022.10:g.42024982_42024993del	NC_000022.10:g.42024983_42024993del	NC_000022.10:g.42024984_42024993del	NC_000022.10:g.42024985_42024993del	NC_000022.10:g.42024986_42024993del	NC_000022.10:g.42024987_42024993del	NC_000022.10:g.42024988_42024993del	NC_000022.10:g.42024989_42024993del	NC_000022.10:g.42024990_42024993del	NC_000022.10:g.42024991_42024993del	NC_000022.10:g.42024992_42024993del	NC_000022.10:g.42024993del	NC_000022.10:g.42024993dup	NC_000022.10:g.42024992_42024993dup	NC_000022.10:g.42024991_42024993dup	NC_000022.10:g.42024990_42024993dup	NC_000022.10:g.42024989_42024993dup	NC_000022.10:g.42024988_42024993dup	NC_000022.10:g.42024987_42024993dup	NC_000022.10:g.42024986_42024993dup	NC_000022.10:g.42024985_42024993dup	NC_000022.10:g.42024978_42024993dup	NC_000022.10:g.42024971_42024993dup	NC_000022.10:g.42024993_42024994insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant 2	NM_001288976.2:c.195+736=	NM_001288976.2:c.195+746_195+759del	NM_001288976.2:c.195+748_195+759del	NM_001288976.2:c.195+749_195+759del	NM_001288976.2:c.195+750_195+759del	NM_001288976.2:c.195+751_195+759del	NM_001288976.2:c.195+752_195+759del	NM_001288976.2:c.195+753_195+759del	NM_001288976.2:c.195+754_195+759del	NM_001288976.2:c.195+755_195+759del	NM_001288976.2:c.195+756_195+759del	NM_001288976.2:c.195+757_195+759del	NM_001288976.2:c.195+758_195+759del	NM_001288976.2:c.195+759del	NM_001288976.2:c.195+759dup	NM_001288976.2:c.195+758_195+759dup	NM_001288976.2:c.195+757_195+759dup	NM_001288976.2:c.195+756_195+759dup	NM_001288976.2:c.195+755_195+759dup	NM_001288976.2:c.195+754_195+759dup	NM_001288976.2:c.195+753_195+759dup	NM_001288976.2:c.195+752_195+759dup	NM_001288976.2:c.195+751_195+759dup	NM_001288976.2:c.195+744_195+759dup	NM_001288976.2:c.195+737_195+759dup	NM_001288976.2:c.195+759_195+760insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant 3	NM_001288977.2:c.195+736=	NM_001288977.2:c.195+746_195+759del	NM_001288977.2:c.195+748_195+759del	NM_001288977.2:c.195+749_195+759del	NM_001288977.2:c.195+750_195+759del	NM_001288977.2:c.195+751_195+759del	NM_001288977.2:c.195+752_195+759del	NM_001288977.2:c.195+753_195+759del	NM_001288977.2:c.195+754_195+759del	NM_001288977.2:c.195+755_195+759del	NM_001288977.2:c.195+756_195+759del	NM_001288977.2:c.195+757_195+759del	NM_001288977.2:c.195+758_195+759del	NM_001288977.2:c.195+759del	NM_001288977.2:c.195+759dup	NM_001288977.2:c.195+758_195+759dup	NM_001288977.2:c.195+757_195+759dup	NM_001288977.2:c.195+756_195+759dup	NM_001288977.2:c.195+755_195+759dup	NM_001288977.2:c.195+754_195+759dup	NM_001288977.2:c.195+753_195+759dup	NM_001288977.2:c.195+752_195+759dup	NM_001288977.2:c.195+751_195+759dup	NM_001288977.2:c.195+744_195+759dup	NM_001288977.2:c.195+737_195+759dup	NM_001288977.2:c.195+759_195+760insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant 4	NM_001288978.2:c.45+6880=	NM_001288978.2:c.45+6890_45+6903del	NM_001288978.2:c.45+6892_45+6903del	NM_001288978.2:c.45+6893_45+6903del	NM_001288978.2:c.45+6894_45+6903del	NM_001288978.2:c.45+6895_45+6903del	NM_001288978.2:c.45+6896_45+6903del	NM_001288978.2:c.45+6897_45+6903del	NM_001288978.2:c.45+6898_45+6903del	NM_001288978.2:c.45+6899_45+6903del	NM_001288978.2:c.45+6900_45+6903del	NM_001288978.2:c.45+6901_45+6903del	NM_001288978.2:c.45+6902_45+6903del	NM_001288978.2:c.45+6903del	NM_001288978.2:c.45+6903dup	NM_001288978.2:c.45+6902_45+6903dup	NM_001288978.2:c.45+6901_45+6903dup	NM_001288978.2:c.45+6900_45+6903dup	NM_001288978.2:c.45+6899_45+6903dup	NM_001288978.2:c.45+6898_45+6903dup	NM_001288978.2:c.45+6897_45+6903dup	NM_001288978.2:c.45+6896_45+6903dup	NM_001288978.2:c.45+6895_45+6903dup	NM_001288978.2:c.45+6888_45+6903dup	NM_001288978.2:c.45+6881_45+6903dup	NM_001288978.2:c.45+6903_45+6904insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript	NM_001469.3:c.195+736=	NM_001469.3:c.195+746_195+759del	NM_001469.3:c.195+748_195+759del	NM_001469.3:c.195+749_195+759del	NM_001469.3:c.195+750_195+759del	NM_001469.3:c.195+751_195+759del	NM_001469.3:c.195+752_195+759del	NM_001469.3:c.195+753_195+759del	NM_001469.3:c.195+754_195+759del	NM_001469.3:c.195+755_195+759del	NM_001469.3:c.195+756_195+759del	NM_001469.3:c.195+757_195+759del	NM_001469.3:c.195+758_195+759del	NM_001469.3:c.195+759del	NM_001469.3:c.195+759dup	NM_001469.3:c.195+758_195+759dup	NM_001469.3:c.195+757_195+759dup	NM_001469.3:c.195+756_195+759dup	NM_001469.3:c.195+755_195+759dup	NM_001469.3:c.195+754_195+759dup	NM_001469.3:c.195+753_195+759dup	NM_001469.3:c.195+752_195+759dup	NM_001469.3:c.195+751_195+759dup	NM_001469.3:c.195+744_195+759dup	NM_001469.3:c.195+737_195+759dup	NM_001469.3:c.195+759_195+760insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant 1	NM_001469.5:c.195+736=	NM_001469.5:c.195+746_195+759del	NM_001469.5:c.195+748_195+759del	NM_001469.5:c.195+749_195+759del	NM_001469.5:c.195+750_195+759del	NM_001469.5:c.195+751_195+759del	NM_001469.5:c.195+752_195+759del	NM_001469.5:c.195+753_195+759del	NM_001469.5:c.195+754_195+759del	NM_001469.5:c.195+755_195+759del	NM_001469.5:c.195+756_195+759del	NM_001469.5:c.195+757_195+759del	NM_001469.5:c.195+758_195+759del	NM_001469.5:c.195+759del	NM_001469.5:c.195+759dup	NM_001469.5:c.195+758_195+759dup	NM_001469.5:c.195+757_195+759dup	NM_001469.5:c.195+756_195+759dup	NM_001469.5:c.195+755_195+759dup	NM_001469.5:c.195+754_195+759dup	NM_001469.5:c.195+753_195+759dup	NM_001469.5:c.195+752_195+759dup	NM_001469.5:c.195+751_195+759dup	NM_001469.5:c.195+744_195+759dup	NM_001469.5:c.195+737_195+759dup	NM_001469.5:c.195+759_195+760insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant X1	XM_005261487.1:c.195+736=	XM_005261487.1:c.195+746_195+759del	XM_005261487.1:c.195+748_195+759del	XM_005261487.1:c.195+749_195+759del	XM_005261487.1:c.195+750_195+759del	XM_005261487.1:c.195+751_195+759del	XM_005261487.1:c.195+752_195+759del	XM_005261487.1:c.195+753_195+759del	XM_005261487.1:c.195+754_195+759del	XM_005261487.1:c.195+755_195+759del	XM_005261487.1:c.195+756_195+759del	XM_005261487.1:c.195+757_195+759del	XM_005261487.1:c.195+758_195+759del	XM_005261487.1:c.195+759del	XM_005261487.1:c.195+759dup	XM_005261487.1:c.195+758_195+759dup	XM_005261487.1:c.195+757_195+759dup	XM_005261487.1:c.195+756_195+759dup	XM_005261487.1:c.195+755_195+759dup	XM_005261487.1:c.195+754_195+759dup	XM_005261487.1:c.195+753_195+759dup	XM_005261487.1:c.195+752_195+759dup	XM_005261487.1:c.195+751_195+759dup	XM_005261487.1:c.195+744_195+759dup	XM_005261487.1:c.195+737_195+759dup	XM_005261487.1:c.195+759_195+760insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant X2	XM_005261488.1:c.195+736=	XM_005261488.1:c.195+746_195+759del	XM_005261488.1:c.195+748_195+759del	XM_005261488.1:c.195+749_195+759del	XM_005261488.1:c.195+750_195+759del	XM_005261488.1:c.195+751_195+759del	XM_005261488.1:c.195+752_195+759del	XM_005261488.1:c.195+753_195+759del	XM_005261488.1:c.195+754_195+759del	XM_005261488.1:c.195+755_195+759del	XM_005261488.1:c.195+756_195+759del	XM_005261488.1:c.195+757_195+759del	XM_005261488.1:c.195+758_195+759del	XM_005261488.1:c.195+759del	XM_005261488.1:c.195+759dup	XM_005261488.1:c.195+758_195+759dup	XM_005261488.1:c.195+757_195+759dup	XM_005261488.1:c.195+756_195+759dup	XM_005261488.1:c.195+755_195+759dup	XM_005261488.1:c.195+754_195+759dup	XM_005261488.1:c.195+753_195+759dup	XM_005261488.1:c.195+752_195+759dup	XM_005261488.1:c.195+751_195+759dup	XM_005261488.1:c.195+744_195+759dup	XM_005261488.1:c.195+737_195+759dup	XM_005261488.1:c.195+759_195+760insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant X3	XM_005261489.1:c.45+6880=	XM_005261489.1:c.45+6890_45+6903del	XM_005261489.1:c.45+6892_45+6903del	XM_005261489.1:c.45+6893_45+6903del	XM_005261489.1:c.45+6894_45+6903del	XM_005261489.1:c.45+6895_45+6903del	XM_005261489.1:c.45+6896_45+6903del	XM_005261489.1:c.45+6897_45+6903del	XM_005261489.1:c.45+6898_45+6903del	XM_005261489.1:c.45+6899_45+6903del	XM_005261489.1:c.45+6900_45+6903del	XM_005261489.1:c.45+6901_45+6903del	XM_005261489.1:c.45+6902_45+6903del	XM_005261489.1:c.45+6903del	XM_005261489.1:c.45+6903dup	XM_005261489.1:c.45+6902_45+6903dup	XM_005261489.1:c.45+6901_45+6903dup	XM_005261489.1:c.45+6900_45+6903dup	XM_005261489.1:c.45+6899_45+6903dup	XM_005261489.1:c.45+6898_45+6903dup	XM_005261489.1:c.45+6897_45+6903dup	XM_005261489.1:c.45+6896_45+6903dup	XM_005261489.1:c.45+6895_45+6903dup	XM_005261489.1:c.45+6888_45+6903dup	XM_005261489.1:c.45+6881_45+6903dup	XM_005261489.1:c.45+6903_45+6904insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XRCC6 transcript variant X1	XM_047441304.1:c.45+6880=	XM_047441304.1:c.45+6890_45+6903del	XM_047441304.1:c.45+6892_45+6903del	XM_047441304.1:c.45+6893_45+6903del	XM_047441304.1:c.45+6894_45+6903del	XM_047441304.1:c.45+6895_45+6903del	XM_047441304.1:c.45+6896_45+6903del	XM_047441304.1:c.45+6897_45+6903del	XM_047441304.1:c.45+6898_45+6903del	XM_047441304.1:c.45+6899_45+6903del	XM_047441304.1:c.45+6900_45+6903del	XM_047441304.1:c.45+6901_45+6903del	XM_047441304.1:c.45+6902_45+6903del	XM_047441304.1:c.45+6903del	XM_047441304.1:c.45+6903dup	XM_047441304.1:c.45+6902_45+6903dup	XM_047441304.1:c.45+6901_45+6903dup	XM_047441304.1:c.45+6900_45+6903dup	XM_047441304.1:c.45+6899_45+6903dup	XM_047441304.1:c.45+6898_45+6903dup	XM_047441304.1:c.45+6897_45+6903dup	XM_047441304.1:c.45+6896_45+6903dup	XM_047441304.1:c.45+6895_45+6903dup	XM_047441304.1:c.45+6888_45+6903dup	XM_047441304.1:c.45+6881_45+6903dup	XM_047441304.1:c.45+6903_45+6904insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

47 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41514781	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95758942	Oct 12, 2018 (152)
3	PJP	ss295080452	May 09, 2011 (138)
4	SSMP	ss664528493	Apr 01, 2015 (144)
5	SWEGEN	ss3019369472	Nov 08, 2017 (151)
6	MCHAISSO	ss3064888847	Nov 08, 2017 (151)
7	URBANLAB	ss3651186965	Oct 12, 2018 (152)
8	EVA_DECODE	ss3708280574	Jul 13, 2019 (153)
9	EVA_DECODE	ss3708280575	Jul 13, 2019 (153)
10	EVA_DECODE	ss3708280576	Jul 13, 2019 (153)
11	GNOMAD	ss4365305360	Apr 27, 2021 (155)
12	GNOMAD	ss4365305361	Apr 27, 2021 (155)
13	GNOMAD	ss4365305362	Apr 27, 2021 (155)
14	GNOMAD	ss4365305363	Apr 27, 2021 (155)
15	GNOMAD	ss4365305364	Apr 27, 2021 (155)
16	GNOMAD	ss4365305365	Apr 27, 2021 (155)
17	GNOMAD	ss4365305366	Apr 27, 2021 (155)
18	GNOMAD	ss4365305367	Apr 27, 2021 (155)
19	GNOMAD	ss4365305368	Apr 27, 2021 (155)
20	GNOMAD	ss4365305369	Apr 27, 2021 (155)
21	GNOMAD	ss4365305370	Apr 27, 2021 (155)
22	GNOMAD	ss4365305371	Apr 27, 2021 (155)
23	GNOMAD	ss4365305373	Apr 27, 2021 (155)
24	GNOMAD	ss4365305374	Apr 27, 2021 (155)
25	GNOMAD	ss4365305375	Apr 27, 2021 (155)
26	GNOMAD	ss4365305376	Apr 27, 2021 (155)
27	GNOMAD	ss4365305377	Apr 27, 2021 (155)
28	GNOMAD	ss4365305378	Apr 27, 2021 (155)
29	GNOMAD	ss4365305379	Apr 27, 2021 (155)
30	GNOMAD	ss4365305380	Apr 27, 2021 (155)
31	GNOMAD	ss4365305381	Apr 27, 2021 (155)
32	TOPMED	ss5110651370	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5232819870	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5232819871	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5232819872	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5232819873	Apr 27, 2021 (155)
37	HUGCELL_USP	ss5503071895	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5503071896	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5503071897	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5794005948	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5794005949	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5794005950	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5794005952	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5794005953	Oct 16, 2022 (156)
45	EVA	ss5822126678	Oct 16, 2022 (156)
46	EVA	ss5822126679	Oct 16, 2022 (156)
47	EVA	ss5853408818	Oct 16, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571162265 (NC_000022.11:41628965::A 44798/59878) Row 571162266 (NC_000022.11:41628965::AA 1886/59364) Row 571162267 (NC_000022.11:41628965::AAA 322/59428)...	-	Apr 27, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 90789177 (NC_000022.10:42024969::A 8609/14580) Row 90789178 (NC_000022.10:42024969::AA 238/14580) Row 90789179 (NC_000022.10:42024969::AAA 637/14580)...	-	Apr 27, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 90789177 (NC_000022.10:42024969::A 8609/14580) Row 90789178 (NC_000022.10:42024969::AA 238/14580) Row 90789179 (NC_000022.10:42024969::AAA 637/14580)...	-	Apr 27, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 90789177 (NC_000022.10:42024969::A 8609/14580) Row 90789178 (NC_000022.10:42024969::AA 238/14580) Row 90789179 (NC_000022.10:42024969::AAA 637/14580)...	-	Apr 27, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 90789177 (NC_000022.10:42024969::A 8609/14580) Row 90789178 (NC_000022.10:42024969::AA 238/14580) Row 90789179 (NC_000022.10:42024969::AAA 637/14580)...	-	Apr 27, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 127843052 (NC_000022.11:41628965::A 15724/24628) Row 127843053 (NC_000022.11:41628965::AA 357/24628) Row 127843054 (NC_000022.11:41628965::AAA 782/24628)...	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 127843052 (NC_000022.11:41628965::A 15724/24628) Row 127843053 (NC_000022.11:41628965::AA 357/24628) Row 127843054 (NC_000022.11:41628965::AAA 782/24628)...	-	Oct 16, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 127843052 (NC_000022.11:41628965::A 15724/24628) Row 127843053 (NC_000022.11:41628965::AA 357/24628) Row 127843054 (NC_000022.11:41628965::AAA 782/24628)...	-	Oct 16, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 127843052 (NC_000022.11:41628965::A 15724/24628) Row 127843053 (NC_000022.11:41628965::AA 357/24628) Row 127843054 (NC_000022.11:41628965::AAA 782/24628)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 127843052 (NC_000022.11:41628965::A 15724/24628) Row 127843053 (NC_000022.11:41628965::AA 357/24628) Row 127843054 (NC_000022.11:41628965::AAA 782/24628)...	-	Oct 16, 2022 (156)
79	TopMed	NC_000022.11 - 41628966	Apr 27, 2021 (155)
80	ALFA	NC_000022.11 - 41628966	Apr 27, 2021 (155)

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

Associated ID	History Updated (Build)
rs35204078	May 15, 2013 (138)
rs71184822	May 11, 2012 (137)
rs145664563	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4365305381	NC_000022.11:41628965:AAAAAAAAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
385760317, ss4365305380, ss5110651370	NC_000022.11:41628965:AAAAAAAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4365305379	NC_000022.11:41628965:AAAAAAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4365305378	NC_000022.11:41628965:AAAAAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4365305377	NC_000022.11:41628965:AAAAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4365305376	NC_000022.11:41628965:AAAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4365305375	NC_000022.11:41628965:AAAAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4365305374	NC_000022.11:41628965:AAAA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305373	NC_000022.11:41628965:AA:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3019369472	NC_000022.10:42024969:A:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3708280576, ss5503071897, ss5794005953	NC_000022.11:41628965:A:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss41514781	NT_011520.12:21415538:A:	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss295080452	NC_000022.9:40354939::A	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss664528493, ss5232819870	NC_000022.10:42024969::A	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3064888847, ss3651186965, ss4365305360, ss5503071895, ss5794005948, ss5853408818	NC_000022.11:41628965::A	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3708280575	NC_000022.11:41628966::A	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95758942	NT_011520.12:21415562::A	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5232819871, ss5822126678	NC_000022.10:42024969::AA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305361, ss5503071896, ss5794005949	NC_000022.11:41628965::AA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3708280574	NC_000022.11:41628966::AA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5232819872, ss5822126679	NC_000022.10:42024969::AAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305362, ss5794005950	NC_000022.11:41628965::AAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305363, ss5794005952	NC_000022.11:41628965::AAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305364	NC_000022.11:41628965::AAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305365	NC_000022.11:41628965::AAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13206393991	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5232819873	NC_000022.10:42024969::AAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305366	NC_000022.11:41628965::AAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305367	NC_000022.11:41628965::AAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305368	NC_000022.11:41628965::AAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305369	NC_000022.11:41628965::AAAAAAAAAAA… NC_000022.11:41628965::AAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305370	NC_000022.11:41628965::AAAAAAAAAAA… NC_000022.11:41628965::AAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4365305371	NC_000022.11:41628965::AAAAAAAAAAA… NC_000022.11:41628965::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:41628965:AAAAAAAAAAAA… NC_000022.11:41628965:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11413169

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

rs11413169