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rs397507266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507266(A;A)
Make rs397507266(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332731
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507266
ebirs397507266
HLIrs397507266
Exacrs397507266
Varsomers397507266
Maprs397507266
PheGenIrs397507266
hapmaprs397507266
1000 genomesrs397507266
hgdprs397507266
ensemblrs397507266
gopubmedrs397507266
geneviewrs397507266
scholarrs397507266
googlers397507266
pharmgkbrs397507266
gwascentralrs397507266
openSNPrs397507266
23andMers397507266
23andMe allrs397507266
SNP Nexus

SNPshotrs397507266
SNPdbers397507266
MSV3drs397507266
GWAS Ctlgrs397507266
Max Magnitude0
ClinVar
Risk rs397507266(A;A)
Alt rs397507266(A;A)
Reference rs397507266(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906868C>A
CLNSRC ClinVar
CLNACC RCV000031313.3,