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rs762648843

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762648843(A;A)
Make rs762648843(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132618295
GeneRAD50
is asnp
is mentioned by
dbSNPrs762648843
ebirs762648843
HLIrs762648843
Exacrs762648843
Varsomers762648843
Maprs762648843
PheGenIrs762648843
hapmaprs762648843
1000 genomesrs762648843
hgdprs762648843
ensemblrs762648843
gopubmedrs762648843
geneviewrs762648843
scholarrs762648843
googlers762648843
pharmgkbrs762648843
gwascentralrs762648843
openSNPrs762648843
23andMers762648843
23andMe allrs762648843
SNP Nexus

SNPshotrs762648843
SNPdbers762648843
MSV3drs762648843
GWAS Ctlgrs762648843
Max Magnitude0
ClinVar
Risk rs762648843(A;A)
Alt rs762648843(A;A)
Reference rs762648843(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131953987G>A
CLNSRC
CLNACC RCV000223643.1,