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rs397507949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507949(G;G)
Make rs397507949(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363182
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507949
ebirs397507949
HLIrs397507949
Exacrs397507949
Varsomers397507949
Maprs397507949
PheGenIrs397507949
hapmaprs397507949
1000 genomesrs397507949
hgdprs397507949
ensemblrs397507949
gopubmedrs397507949
geneviewrs397507949
scholarrs397507949
googlers397507949
pharmgkbrs397507949
gwascentralrs397507949
openSNPrs397507949
23andMers397507949
23andMe allrs397507949
SNP Nexus

SNPshotrs397507949
SNPdbers397507949
MSV3drs397507949
GWAS Ctlgrs397507949
Max Magnitude0
ClinVar
Risk rs397507949(C,G;C,G)
Alt rs397507949(C,G;C,G)
Reference rs397507949(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937319T>C; NC_000013.10:g.32937319T>G
CLNSRC ClinVar
CLNACC RCV000163208.1, RCV000045372.2, RCV000225390.1,