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rs397507867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 6 BRCA2 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar
(C;G) 6 BRCA2 variant considered pathogenic for breast cancer


Make rs397507867(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340912
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507867
ClinGenrs397507867
ebirs397507867
HLIrs397507867
Exacrs397507867
Varsomers397507867
Maprs397507867
PheGenIrs397507867
hapmaprs397507867
1000 genomesrs397507867
hgdprs397507867
ensemblrs397507867
gopubmedrs397507867
geneviewrs397507867
scholarrs397507867
googlers397507867
pharmgkbrs397507867
gwascentralrs397507867
openSNPrs397507867
23andMers397507867
23andMe allrs397507867
SNP Nexus

SNPshotrs397507867
SNPdbers397507867
MSV3drs397507867
GWAS Ctlgrs397507867
Max Magnitude6
ClinVar
Risk rs397507867(A;A) rs397507867(G;G) rs397507867(T;T)
Alt rs397507867(A;A) rs397507867(G;G) rs397507867(T;T)
Reference Rs397507867(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32915049C>A; NC_000013.10:g.32915049C>G; NC_000013.10:g.32915049C>T
CLNSRC ClinVar
CLNACC RCV000044984.2, RCV000241520.2, RCV000257527.2, RCV000475735.1,