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rs397508033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508033(-;-)
Make rs397508033(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332384
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508033
ebirs397508033
HLIrs397508033
Exacrs397508033
Varsomers397508033
Maprs397508033
PheGenIrs397508033
hapmaprs397508033
1000 genomesrs397508033
hgdprs397508033
ensemblrs397508033
gopubmedrs397508033
geneviewrs397508033
scholarrs397508033
googlers397508033
pharmgkbrs397508033
gwascentralrs397508033
openSNPrs397508033
23andMers397508033
23andMe allrs397508033
SNP Nexus

SNPshotrs397508033
SNPdbers397508033
MSV3drs397508033
GWAS Ctlgrs397508033
Max Magnitude0
ClinVar
Risk rs397508033(;)
Alt rs397508033(;)
Reference rs397508033(C;C)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906521delC
CLNSRC ClinVar
CLNACC RCV000045703.2, RCV000215368.1, RCV000225415.1,