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rs587782036

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782036(C;C)
Make rs587782036(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58696692
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782036
ebirs587782036
HLIrs587782036
Exacrs587782036
Varsomers587782036
Maprs587782036
PheGenIrs587782036
hapmaprs587782036
1000 genomesrs587782036
hgdprs587782036
ensemblrs587782036
gopubmedrs587782036
geneviewrs587782036
scholarrs587782036
googlers587782036
pharmgkbrs587782036
gwascentralrs587782036
openSNPrs587782036
23andMers587782036
23andMe allrs587782036
SNP Nexus

SNPshotrs587782036
SNPdbers587782036
MSV3drs587782036
GWAS Ctlgrs587782036
Max Magnitude0
ClinVar
Risk rs587782036(C;C)
Alt rs587782036(C;C)
Reference rs587782036(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Fanconi anemia
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56774053G>C
CLNSRC
CLNACC RCV000130492.2, RCV000204135.1,