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rs397507357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507357(-;-)
Make rs397507357(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339986
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507357
ebirs397507357
HLIrs397507357
Exacrs397507357
Varsomers397507357
Maprs397507357
PheGenIrs397507357
hapmaprs397507357
1000 genomesrs397507357
hgdprs397507357
ensemblrs397507357
gopubmedrs397507357
geneviewrs397507357
scholarrs397507357
googlers397507357
pharmgkbrs397507357
gwascentralrs397507357
openSNPrs397507357
23andMers397507357
23andMe allrs397507357
SNP Nexus

SNPshotrs397507357
SNPdbers397507357
MSV3drs397507357
GWAS Ctlgrs397507357
Max Magnitude0
ClinVar
Risk rs397507357(;)
Alt rs397507357(;)
Reference rs397507357(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914123delC
CLNSRC ClinVar
CLNACC RCV000031562.3, RCV000166635.1,