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rs760235677

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760235677(A;A)
Make rs760235677(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58709991
GeneRAD51C
is asnp
is mentioned by
dbSNPrs760235677
ebirs760235677
HLIrs760235677
Exacrs760235677
Varsomers760235677
Maprs760235677
PheGenIrs760235677
hapmaprs760235677
1000 genomesrs760235677
hgdprs760235677
ensemblrs760235677
gopubmedrs760235677
geneviewrs760235677
scholarrs760235677
googlers760235677
pharmgkbrs760235677
gwascentralrs760235677
openSNPrs760235677
23andMers760235677
23andMe allrs760235677
SNP Nexus

SNPshotrs760235677
SNPdbers760235677
MSV3drs760235677
GWAS Ctlgrs760235677
Max Magnitude0
ClinVar
Risk rs760235677(A;A)
Alt rs760235677(A;A)
Reference rs760235677(G;G)
Significance 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.56787352G>A; NC_000017.10:g.56787352G>T
CLNSRC
CLNACC RCV000221081.1, RCV000226369.1,