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rs397508003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AA) 6 BRCA2 variant considered pathogenic for breast cancer
(AA;AA) 0 common in clinvar


Make rs397508003(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376754
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508003
dbSNP (old)rs397508003
ClinGenrs397508003
ebirs397508003
HLIrs397508003
Exacrs397508003
Gnomadrs397508003
Varsomers397508003
Maprs397508003
PheGenIrs397508003
Biobankrs397508003
1000 genomesrs397508003
hgdprs397508003
ensemblrs397508003
gopubmedrs397508003
geneviewrs397508003
scholarrs397508003
googlers397508003
pharmgkbrs397508003
gwascentralrs397508003
openSNPrs397508003
23andMers397508003
23andMe allrs397508003
SNP Nexus

SNPshotrs397508003
SNPdbers397508003
MSV3drs397508003
GWAS Ctlgrs397508003
Max Magnitude6
ClinVar
Risk rs397508003(-;-)
Alt rs397508003(-;-)
Reference Rs397508003(AA;AA)
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.32950891_32950892delAA
CLNSRC ClinVar
CLNACC RCV000045607.2, RCV000257064.2,