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rs397507303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507303(A;A)
Make rs397507303(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319326
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507303
ebirs397507303
HLIrs397507303
Exacrs397507303
Varsomers397507303
Maprs397507303
PheGenIrs397507303
hapmaprs397507303
1000 genomesrs397507303
hgdprs397507303
ensemblrs397507303
gopubmedrs397507303
geneviewrs397507303
scholarrs397507303
googlers397507303
pharmgkbrs397507303
gwascentralrs397507303
openSNPrs397507303
23andMers397507303
23andMe allrs397507303
SNP Nexus

SNPshotrs397507303
SNPdbers397507303
MSV3drs397507303
GWAS Ctlgrs397507303
Max Magnitude0
ClinVar
Risk rs397507303(A,C,T;A,C,T)
Alt rs397507303(A,C,T;A,C,T)
Reference rs397507303(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32893463G>A; NC_000013.10:g.32893463G>C; NC_000013.10:g.32893463G>T
CLNSRC ClinVar
CLNACC RCV000031403.3, RCV000031404.3, RCV000165392.1,