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rs121917739

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917739(A;A)
Make rs121917739(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position40718818
GeneRAD51
is asnp
is mentioned by
dbSNPrs121917739
ebirs121917739
HLIrs121917739
Exacrs121917739
Varsomers121917739
Maprs121917739
PheGenIrs121917739
hapmaprs121917739
1000 genomesrs121917739
hgdprs121917739
ensemblrs121917739
gopubmedrs121917739
geneviewrs121917739
scholarrs121917739
googlers121917739
pharmgkbrs121917739
gwascentralrs121917739
openSNPrs121917739
23andMers121917739
23andMe allrs121917739
SNP Nexus

SNPshotrs121917739
SNPdbers121917739
MSV3drs121917739
GWAS Ctlgrs121917739
GMAF0.002296
Max Magnitude0
OMIM179617
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121917739(A;A)
Alt rs121917739(A;A)
Reference rs121917739(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene RAD51
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000015.9:g.41011016G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014007.17,