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rs397507967

From SNPedia

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


Make rs397507967(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363397
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507967
dbSNP (old)rs397507967
ClinGenrs397507967
ebirs397507967
HLIrs397507967
Exacrs397507967
Gnomadrs397507967
Varsomers397507967
Maprs397507967
PheGenIrs397507967
Biobankrs397507967
1000 genomesrs397507967
hgdprs397507967
ensemblrs397507967
gopubmedrs397507967
geneviewrs397507967
scholarrs397507967
googlers397507967
pharmgkbrs397507967
gwascentralrs397507967
openSNPrs397507967
23andMers397507967
23andMe allrs397507967
SNP Nexus

SNPshotrs397507967
SNPdbers397507967
MSV3drs397507967
GWAS Ctlgrs397507967
Max Magnitude6
ClinVar
Risk rs397507967(A;A) rs397507967(G;G)
Alt rs397507967(A;A) rs397507967(G;G)
Reference Rs397507967(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Neoplasm of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Neoplasm of breast
Reversed 0
HGVS NC_000013.10:g.32937534T>A; NC_000013.10:g.32937534T>G
CLNSRC ClinVar
CLNACC RCV000257040.1, RCV000045450.2, RCV000257547.2, RCV000412877.1,