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rs397507284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507284(-;-)
Make rs397507284(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336679
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507284
ebirs397507284
HLIrs397507284
Exacrs397507284
Varsomers397507284
Maprs397507284
PheGenIrs397507284
hapmaprs397507284
1000 genomesrs397507284
hgdprs397507284
ensemblrs397507284
gopubmedrs397507284
geneviewrs397507284
scholarrs397507284
googlers397507284
pharmgkbrs397507284
gwascentralrs397507284
openSNPrs397507284
23andMers397507284
23andMe allrs397507284
SNP Nexus

SNPshotrs397507284
SNPdbers397507284
MSV3drs397507284
GWAS Ctlgrs397507284
Max Magnitude0
ClinVar
Risk rs397507284(;)
Alt rs397507284(;)
Reference rs397507284(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910816delC
CLNSRC ClinVar
CLNACC RCV000031363.3,