Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508009(G;T)
Make rs397508009(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332358
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508009
ebirs397508009
HLIrs397508009
Exacrs397508009
Varsomers397508009
Maprs397508009
PheGenIrs397508009
hapmaprs397508009
1000 genomesrs397508009
hgdprs397508009
ensemblrs397508009
gopubmedrs397508009
geneviewrs397508009
scholarrs397508009
googlers397508009
pharmgkbrs397508009
gwascentralrs397508009
openSNPrs397508009
23andMers397508009
23andMe allrs397508009
SNP Nexus

SNPshotrs397508009
SNPdbers397508009
MSV3drs397508009
GWAS Ctlgrs397508009
Max Magnitude0
ClinVar
Risk rs397508009(T;T)
Alt rs397508009(T;T)
Reference rs397508009(G;G)
Significance Other
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.32906495G>T
CLNSRC ClinVar Counsyl
CLNACC RCV000045632.2, RCV000077453.5,