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rs876659874

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659874(A;A)
Make rs876659874(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58724049
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs876659874
ebirs876659874
HLIrs876659874
Exacrs876659874
Varsomers876659874
Maprs876659874
PheGenIrs876659874
hapmaprs876659874
1000 genomesrs876659874
hgdprs876659874
ensemblrs876659874
gopubmedrs876659874
geneviewrs876659874
scholarrs876659874
googlers876659874
pharmgkbrs876659874
gwascentralrs876659874
openSNPrs876659874
23andMers876659874
23andMe allrs876659874
SNP Nexus

SNPshotrs876659874
SNPdbers876659874
MSV3drs876659874
GWAS Ctlgrs876659874
Max Magnitude0
ClinVar
Risk rs876659874(A;A)
Alt rs876659874(A;A)
Reference rs876659874(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene RAD51C
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000017.10:g.56801410G>A
CLNSRC
CLNACC RCV000221970.1, RCV000236899.1,