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rs587781410

From SNPedia

Orientationplus
Geno Mag Summary
(AGT;AGT) 0 common in clinvar
Make rs587781410(-;-)
Make rs587781410(-;GTA)
Make rs587781410(GTA;GTA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58732549
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs587781410
ebirs587781410
HLIrs587781410
Exacrs587781410
Varsomers587781410
Maprs587781410
PheGenIrs587781410
hapmaprs587781410
1000 genomesrs587781410
hgdprs587781410
ensemblrs587781410
gopubmedrs587781410
geneviewrs587781410
scholarrs587781410
googlers587781410
pharmgkbrs587781410
gwascentralrs587781410
openSNPrs587781410
23andMers587781410
23andMe allrs587781410
SNP Nexus

SNPshotrs587781410
SNPdbers587781410
MSV3drs587781410
GWAS Ctlgrs587781410
Max Magnitude0
Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312OA-icon.png]
ClinVar
Risk rs587781410(;)
Alt rs587781410(;)
Reference rs587781410(AGT;AGT)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed 0
HGVS NC_000017.10:g.56809910_56809912delGTA
CLNSRC
CLNACC RCV000116170.6, RCV000197293.3, RCV000235204.1,