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rs587782818

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782818(C;G)
Make rs587782818(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58703325
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782818
ebirs587782818
HLIrs587782818
Exacrs587782818
Varsomers587782818
Maprs587782818
PheGenIrs587782818
hapmaprs587782818
1000 genomesrs587782818
hgdprs587782818
ensemblrs587782818
gopubmedrs587782818
geneviewrs587782818
scholarrs587782818
googlers587782818
pharmgkbrs587782818
gwascentralrs587782818
openSNPrs587782818
23andMers587782818
23andMe allrs587782818
SNP Nexus

SNPshotrs587782818
SNPdbers587782818
MSV3drs587782818
GWAS Ctlgrs587782818
Max Magnitude0
ClinVar
Risk rs587782818(G;G)
Alt rs587782818(G;G)
Reference rs587782818(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.56780686C>G
CLNSRC
CLNACC RCV000132392.2,