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rs587782702

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782702(G;T)
Make rs587782702(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58720817
GeneRAD51C
is asnp
is mentioned by
dbSNPrs587782702
ebirs587782702
HLIrs587782702
Exacrs587782702
Varsomers587782702
Maprs587782702
PheGenIrs587782702
hapmaprs587782702
1000 genomesrs587782702
hgdprs587782702
ensemblrs587782702
gopubmedrs587782702
geneviewrs587782702
scholarrs587782702
googlers587782702
pharmgkbrs587782702
gwascentralrs587782702
openSNPrs587782702
23andMers587782702
23andMe allrs587782702
SNP Nexus

SNPshotrs587782702
SNPdbers587782702
MSV3drs587782702
GWAS Ctlgrs587782702
Max Magnitude0
ClinVar
Risk rs587782702(T;T)
Alt rs587782702(T;T)
Reference rs587782702(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.56798178G>T
CLNSRC
CLNACC RCV000132144.2, RCV000225845.1,