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rs1064795774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position58695010
GeneRAD51C
is asnp
is mentioned by
dbSNPrs1064795774
dbSNP (old)rs1064795774
ClinGenrs1064795774
ebirs1064795774
HLIrs1064795774
Exacrs1064795774
Gnomadrs1064795774
Varsomers1064795774
LitVarrs1064795774
Maprs1064795774
PheGenIrs1064795774
Biobankrs1064795774
1000 genomesrs1064795774
hgdprs1064795774
ensemblrs1064795774
gopubmedrs1064795774
geneviewrs1064795774
scholarrs1064795774
googlers1064795774
pharmgkbrs1064795774
gwascentralrs1064795774
openSNPrs1064795774
23andMers1064795774
23andMe allrs1064795774
SNPshotrs1064795774
SNPdbers1064795774
MSV3drs1064795774
GWAS Ctlgrs1064795774
Max Magnitude0
ClinVar
Risk rs1064795774(-;-)
Alt rs1064795774(-;-)
Reference Rs1064795774(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RAD51C
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.56772371delT
CLNSRC
CLNACC RCV000483240.1,