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

rs397508002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508002(C;T)
Make rs397508002(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376717
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508002
ebirs397508002
HLIrs397508002
Exacrs397508002
Varsomers397508002
Maprs397508002
PheGenIrs397508002
hapmaprs397508002
1000 genomesrs397508002
hgdprs397508002
ensemblrs397508002
gopubmedrs397508002
geneviewrs397508002
scholarrs397508002
googlers397508002
pharmgkbrs397508002
gwascentralrs397508002
openSNPrs397508002
23andMers397508002
23andMe allrs397508002
SNP Nexus

SNPshotrs397508002
SNPdbers397508002
MSV3drs397508002
GWAS Ctlgrs397508002
Max Magnitude0
ClinVar
Risk rs397508002(T;T)
Alt rs397508002(T;T)
Reference rs397508002(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32950854C>T
CLNSRC ClinVar
CLNACC RCV000045601.2,