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rs587782533

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782533(-;-)
Make rs587782533(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58694943
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782533
ebirs587782533
HLIrs587782533
Exacrs587782533
Varsomers587782533
Maprs587782533
PheGenIrs587782533
hapmaprs587782533
1000 genomesrs587782533
hgdprs587782533
ensemblrs587782533
gopubmedrs587782533
geneviewrs587782533
scholarrs587782533
googlers587782533
pharmgkbrs587782533
gwascentralrs587782533
openSNPrs587782533
23andMers587782533
23andMe allrs587782533
SNP Nexus

SNPshotrs587782533
SNPdbers587782533
MSV3drs587782533
GWAS Ctlgrs587782533
Max Magnitude0
ClinVar
Risk rs587782533(;)
Alt rs587782533(;)
Reference rs587782533(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56772304delC
CLNSRC
CLNACC RCV000131735.2,