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rs397507891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507891(C;C)
Make rs397507891(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346897
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507891
ebirs397507891
HLIrs397507891
Exacrs397507891
Varsomers397507891
Maprs397507891
PheGenIrs397507891
hapmaprs397507891
1000 genomesrs397507891
hgdprs397507891
ensemblrs397507891
gopubmedrs397507891
geneviewrs397507891
scholarrs397507891
googlers397507891
pharmgkbrs397507891
gwascentralrs397507891
openSNPrs397507891
23andMers397507891
23andMe allrs397507891
SNP Nexus

SNPshotrs397507891
SNPdbers397507891
MSV3drs397507891
GWAS Ctlgrs397507891
Max Magnitude0
ClinVar
Risk rs397507891(A,C,T;A,C,T)
Alt rs397507891(A,C,T;A,C,T)
Reference rs397507891(G;G)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32921034G>A; NC_000013.10:g.32921034G>C; NC_000013.10:g.32921034G>T
CLNSRC ClinVar
CLNACC RCV000232637.1, RCV000045108.2, RCV000045109.2,