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rs767796996

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767796996(A;A)
Make rs767796996(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58695189
GeneRAD51C
is asnp
is mentioned by
dbSNPrs767796996
ebirs767796996
HLIrs767796996
Exacrs767796996
Varsomers767796996
Maprs767796996
PheGenIrs767796996
hapmaprs767796996
1000 genomesrs767796996
hgdprs767796996
ensemblrs767796996
gopubmedrs767796996
geneviewrs767796996
scholarrs767796996
googlers767796996
pharmgkbrs767796996
gwascentralrs767796996
openSNPrs767796996
23andMers767796996
23andMe allrs767796996
SNP Nexus

SNPshotrs767796996
SNPdbers767796996
MSV3drs767796996
GWAS Ctlgrs767796996
Max Magnitude0
ClinVar
Risk rs767796996(A;A)
Alt rs767796996(A;A)
Reference rs767796996(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD51C
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.56772550G>A
CLNSRC
CLNACC RCV000217463.1,