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rs397507412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507412(G;G)
Make rs397507412(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376793
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507412
ebirs397507412
HLIrs397507412
Exacrs397507412
Varsomers397507412
Maprs397507412
PheGenIrs397507412
hapmaprs397507412
1000 genomesrs397507412
hgdprs397507412
ensemblrs397507412
gopubmedrs397507412
geneviewrs397507412
scholarrs397507412
googlers397507412
pharmgkbrs397507412
gwascentralrs397507412
openSNPrs397507412
23andMers397507412
23andMe allrs397507412
SNP Nexus

SNPshotrs397507412
SNPdbers397507412
MSV3drs397507412
GWAS Ctlgrs397507412
Max Magnitude0
ClinVar
Risk rs397507412(G;G)
Alt rs397507412(G;G)
Reference rs397507412(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.32950930T>G
CLNSRC ClinVar
CLNACC RCV000031764.3,