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rs587782170

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587782170(-;-)
Make rs587782170(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58694971
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782170
ebirs587782170
HLIrs587782170
Exacrs587782170
Varsomers587782170
Maprs587782170
PheGenIrs587782170
hapmaprs587782170
1000 genomesrs587782170
hgdprs587782170
ensemblrs587782170
gopubmedrs587782170
geneviewrs587782170
scholarrs587782170
googlers587782170
pharmgkbrs587782170
gwascentralrs587782170
openSNPrs587782170
23andMers587782170
23andMe allrs587782170
SNP Nexus

SNPshotrs587782170
SNPdbers587782170
MSV3drs587782170
GWAS Ctlgrs587782170
Max Magnitude0
ClinVar
Risk rs587782170(;)
Alt rs587782170(;)
Reference rs587782170(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56772332_56772333delAA
CLNSRC
CLNACC RCV000130769.2,