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rs397507979

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507979(C;C)
Make rs397507979(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370401
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507979
ebirs397507979
HLIrs397507979
Exacrs397507979
Varsomers397507979
Maprs397507979
PheGenIrs397507979
hapmaprs397507979
1000 genomesrs397507979
hgdprs397507979
ensemblrs397507979
gopubmedrs397507979
geneviewrs397507979
scholarrs397507979
googlers397507979
pharmgkbrs397507979
gwascentralrs397507979
openSNPrs397507979
23andMers397507979
23andMe allrs397507979
SNP Nexus

SNPshotrs397507979
SNPdbers397507979
MSV3drs397507979
GWAS Ctlgrs397507979
Max Magnitude0
ClinVar
Risk rs397507979(C,T;C,T)
Alt rs397507979(C,T;C,T)
Reference rs397507979(G;G)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944538G>C; NC_000013.10:g.32944538G>T
CLNSRC ClinVar
CLNACC RCV000045481.2, RCV000164696.1,