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rs397507355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507355(-;-)
Make rs397507355(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339932
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507355
ebirs397507355
HLIrs397507355
Exacrs397507355
Varsomers397507355
Maprs397507355
PheGenIrs397507355
hapmaprs397507355
1000 genomesrs397507355
hgdprs397507355
ensemblrs397507355
gopubmedrs397507355
geneviewrs397507355
scholarrs397507355
googlers397507355
pharmgkbrs397507355
gwascentralrs397507355
openSNPrs397507355
23andMers397507355
23andMe allrs397507355
SNP Nexus

SNPshotrs397507355
SNPdbers397507355
MSV3drs397507355
GWAS Ctlgrs397507355
Max Magnitude0
ClinVar
Risk rs397507355(;)
Alt rs397507355(;)
Reference rs397507355(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914069delT
CLNSRC ClinVar
CLNACC RCV000031557.3,