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rs397508031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508031(-;-)
Make rs397508031(-;G)
Make rs397508031(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332379
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508031
ebirs397508031
HLIrs397508031
Exacrs397508031
Varsomers397508031
Maprs397508031
PheGenIrs397508031
hapmaprs397508031
1000 genomesrs397508031
hgdprs397508031
ensemblrs397508031
gopubmedrs397508031
geneviewrs397508031
scholarrs397508031
googlers397508031
pharmgkbrs397508031
gwascentralrs397508031
openSNPrs397508031
23andMers397508031
23andMe allrs397508031
SNP Nexus

SNPshotrs397508031
SNPdbers397508031
MSV3drs397508031
GWAS Ctlgrs397508031
Max Magnitude0
ClinVar
Risk rs397508031(G;G)
Alt rs397508031(G;G)
Reference rs397508031(;)
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.32906516dupG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045691.2, RCV000112861.1,