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rs397508052

From SNPedia

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


Make rs397508052(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394890
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508052
ClinGenrs397508052
ebirs397508052
HLIrs397508052
Exacrs397508052
Varsomers397508052
Maprs397508052
PheGenIrs397508052
hapmaprs397508052
1000 genomesrs397508052
hgdprs397508052
ensemblrs397508052
gopubmedrs397508052
geneviewrs397508052
scholarrs397508052
googlers397508052
pharmgkbrs397508052
gwascentralrs397508052
openSNPrs397508052
23andMers397508052
23andMe allrs397508052
SNP Nexus

SNPshotrs397508052
SNPdbers397508052
MSV3drs397508052
GWAS Ctlgrs397508052
Max Magnitude6
ClinVar
Risk rs397508052(-;-)
Alt rs397508052(-;-)
Reference Rs397508052(G;G)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32969027delG
CLNSRC ClinVar
CLNACC RCV000045826.2, RCV000218767.1, RCV000241312.2,