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rs397507325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507325(A;A)
Make rs397507325(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338506
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507325
ebirs397507325
HLIrs397507325
Exacrs397507325
Varsomers397507325
Maprs397507325
PheGenIrs397507325
hapmaprs397507325
1000 genomesrs397507325
hgdprs397507325
ensemblrs397507325
gopubmedrs397507325
geneviewrs397507325
scholarrs397507325
googlers397507325
pharmgkbrs397507325
gwascentralrs397507325
openSNPrs397507325
23andMers397507325
23andMe allrs397507325
SNP Nexus

SNPshotrs397507325
SNPdbers397507325
MSV3drs397507325
GWAS Ctlgrs397507325
Max Magnitude0
ClinVar
Risk rs397507325(A;A)
Alt rs397507325(A;A)
Reference rs397507325(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912643T>A
CLNSRC ClinVar
CLNACC RCV000031465.3,