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rs876658652

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658652(-;-)
Make rs876658652(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58724038
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs876658652
ebirs876658652
HLIrs876658652
Exacrs876658652
Varsomers876658652
Maprs876658652
PheGenIrs876658652
hapmaprs876658652
1000 genomesrs876658652
hgdprs876658652
ensemblrs876658652
gopubmedrs876658652
geneviewrs876658652
scholarrs876658652
googlers876658652
pharmgkbrs876658652
gwascentralrs876658652
openSNPrs876658652
23andMers876658652
23andMe allrs876658652
SNP Nexus

SNPshotrs876658652
SNPdbers876658652
MSV3drs876658652
GWAS Ctlgrs876658652
Max Magnitude0
ClinVar
Risk rs876658652(;)
Alt rs876658652(;)
Reference rs876658652(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Fanconi anemia
Variation info
Gene RAD51C
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56801399delA
CLNSRC
CLNACC RCV000221587.1, RCV000229896.1,