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rs587782286

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587782286(-;-)
Make rs587782286(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58703275
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782286
ebirs587782286
HLIrs587782286
Exacrs587782286
Varsomers587782286
Maprs587782286
PheGenIrs587782286
hapmaprs587782286
1000 genomesrs587782286
hgdprs587782286
ensemblrs587782286
gopubmedrs587782286
geneviewrs587782286
scholarrs587782286
googlers587782286
pharmgkbrs587782286
gwascentralrs587782286
openSNPrs587782286
23andMers587782286
23andMe allrs587782286
SNP Nexus

SNPshotrs587782286
SNPdbers587782286
MSV3drs587782286
GWAS Ctlgrs587782286
Max Magnitude0
ClinVar
Risk rs587782286(;)
Alt rs587782286(;)
Reference rs587782286(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56780638_56780639delAG
CLNSRC
CLNACC RCV000166223.2,