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rs397507996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507996(G;T)
Make rs397507996(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371088
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507996
ebirs397507996
HLIrs397507996
Exacrs397507996
Varsomers397507996
Maprs397507996
PheGenIrs397507996
hapmaprs397507996
1000 genomesrs397507996
hgdprs397507996
ensemblrs397507996
gopubmedrs397507996
geneviewrs397507996
scholarrs397507996
googlers397507996
pharmgkbrs397507996
gwascentralrs397507996
openSNPrs397507996
23andMers397507996
23andMe allrs397507996
SNP Nexus

SNPshotrs397507996
SNPdbers397507996
MSV3drs397507996
GWAS Ctlgrs397507996
Max Magnitude0
ClinVar
Risk rs397507996(T;T)
Alt rs397507996(T;T)
Reference rs397507996(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32945225G>T
CLNSRC ClinVar
CLNACC RCV000045574.2, RCV000225505.1,