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rs587780259

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780259(A;G)
Make rs587780259(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58709857
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587780259
ebirs587780259
HLIrs587780259
Exacrs587780259
Varsomers587780259
Maprs587780259
PheGenIrs587780259
hapmaprs587780259
1000 genomesrs587780259
hgdprs587780259
ensemblrs587780259
gopubmedrs587780259
geneviewrs587780259
scholarrs587780259
googlers587780259
pharmgkbrs587780259
gwascentralrs587780259
openSNPrs587780259
23andMers587780259
23andMe allrs587780259
SNP Nexus

SNPshotrs587780259
SNPdbers587780259
MSV3drs587780259
GWAS Ctlgrs587780259
Max Magnitude0
ClinVar
Risk rs587780259(G;G)
Alt rs587780259(G;G)
Reference rs587780259(A;A)
Significance 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.56787218A>G
CLNSRC
CLNACC RCV000116178.4, RCV000234445.1,