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rs397507332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507332(-;-)
Make rs397507332(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338769
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507332
ebirs397507332
HLIrs397507332
Exacrs397507332
Varsomers397507332
Maprs397507332
PheGenIrs397507332
hapmaprs397507332
1000 genomesrs397507332
hgdprs397507332
ensemblrs397507332
gopubmedrs397507332
geneviewrs397507332
scholarrs397507332
googlers397507332
pharmgkbrs397507332
gwascentralrs397507332
openSNPrs397507332
23andMers397507332
23andMe allrs397507332
SNP Nexus

SNPshotrs397507332
SNPdbers397507332
MSV3drs397507332
GWAS Ctlgrs397507332
Max Magnitude0
ClinVar
Risk rs397507332(;)
Alt rs397507332(;)
Reference rs397507332(AA;AA)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912906_32912907delAA
CLNSRC ClinVar
CLNACC RCV000031482.3, RCV000044409.2,