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rs397507305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507305(G;G)
Make rs397507305(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337663
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507305
ebirs397507305
HLIrs397507305
Exacrs397507305
Varsomers397507305
Maprs397507305
PheGenIrs397507305
hapmaprs397507305
1000 genomesrs397507305
hgdprs397507305
ensemblrs397507305
gopubmedrs397507305
geneviewrs397507305
scholarrs397507305
googlers397507305
pharmgkbrs397507305
gwascentralrs397507305
openSNPrs397507305
23andMers397507305
23andMe allrs397507305
SNP Nexus

SNPshotrs397507305
SNPdbers397507305
MSV3drs397507305
GWAS Ctlgrs397507305
Max Magnitude0
ClinVar
Risk rs397507305(G;G)
Alt rs397507305(G;G)
Reference rs397507305(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.32911800T>G
CLNSRC ClinVar
CLNACC RCV000031415.3,