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rs587781287

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781287(C;T)
Make rs587781287(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58724090
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs587781287
ebirs587781287
HLIrs587781287
Exacrs587781287
Varsomers587781287
Maprs587781287
PheGenIrs587781287
hapmaprs587781287
1000 genomesrs587781287
hgdprs587781287
ensemblrs587781287
gopubmedrs587781287
geneviewrs587781287
scholarrs587781287
googlers587781287
pharmgkbrs587781287
gwascentralrs587781287
openSNPrs587781287
23andMers587781287
23andMe allrs587781287
SNP Nexus

SNPshotrs587781287
SNPdbers587781287
MSV3drs587781287
GWAS Ctlgrs587781287
Max Magnitude0
ClinVar
Risk rs587781287(T;T)
Alt rs587781287(T;T)
Reference Rs587781287(C;C)
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.56801451C>T
CLNSRC
CLNACC RCV000128973.3, RCV000230603.1,