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rs397507291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs397507291(-;-)
Make rs397507291(-;TG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337013
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507291
ebirs397507291
HLIrs397507291
Exacrs397507291
Varsomers397507291
Maprs397507291
PheGenIrs397507291
hapmaprs397507291
1000 genomesrs397507291
hgdprs397507291
ensemblrs397507291
gopubmedrs397507291
geneviewrs397507291
scholarrs397507291
googlers397507291
pharmgkbrs397507291
gwascentralrs397507291
openSNPrs397507291
23andMers397507291
23andMe allrs397507291
SNP Nexus

SNPshotrs397507291
SNPdbers397507291
MSV3drs397507291
GWAS Ctlgrs397507291
Max Magnitude0
ClinVar
Risk rs397507291(;)
Alt rs397507291(;)
Reference rs397507291(TG;TG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911150_32911151delTG
CLNSRC ClinVar
CLNACC RCV000031377.3,