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rs397507831

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507831(-;-)
Make rs397507831(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340519
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507831
ebirs397507831
HLIrs397507831
Exacrs397507831
Varsomers397507831
Maprs397507831
PheGenIrs397507831
hapmaprs397507831
1000 genomesrs397507831
hgdprs397507831
ensemblrs397507831
gopubmedrs397507831
geneviewrs397507831
scholarrs397507831
googlers397507831
pharmgkbrs397507831
gwascentralrs397507831
openSNPrs397507831
23andMers397507831
23andMe allrs397507831
SNP Nexus

SNPshotrs397507831
SNPdbers397507831
MSV3drs397507831
GWAS Ctlgrs397507831
Max Magnitude0
ClinVar
Risk rs397507831(;)
Alt rs397507831(;)
Reference rs397507831(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914656delT
CLNSRC ClinVar
CLNACC RCV000044858.3, RCV000239163.1,