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rs759292615

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759292615(A;A)
Make rs759292615(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58732523
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs759292615
ebirs759292615
HLIrs759292615
Exacrs759292615
Varsomers759292615
Maprs759292615
PheGenIrs759292615
hapmaprs759292615
1000 genomesrs759292615
hgdprs759292615
ensemblrs759292615
gopubmedrs759292615
geneviewrs759292615
scholarrs759292615
googlers759292615
pharmgkbrs759292615
gwascentralrs759292615
openSNPrs759292615
23andMers759292615
23andMe allrs759292615
SNP Nexus

SNPshotrs759292615
SNPdbers759292615
MSV3drs759292615
GWAS Ctlgrs759292615
Max Magnitude0
ClinVar
Risk rs759292615(A;A)
Alt rs759292615(A;A)
Reference rs759292615(C;C)
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.56809884C>A
CLNSRC
CLNACC RCV000220031.1, RCV000232127.1,