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rs876660797

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660797(C;T)
Make rs876660797(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132603376
GeneRAD50
is asnp
is mentioned by
dbSNPrs876660797
ebirs876660797
HLIrs876660797
Exacrs876660797
Varsomers876660797
Maprs876660797
PheGenIrs876660797
hapmaprs876660797
1000 genomesrs876660797
hgdprs876660797
ensemblrs876660797
gopubmedrs876660797
geneviewrs876660797
scholarrs876660797
googlers876660797
pharmgkbrs876660797
gwascentralrs876660797
openSNPrs876660797
23andMers876660797
23andMe allrs876660797
SNP Nexus

SNPshotrs876660797
SNPdbers876660797
MSV3drs876660797
GWAS Ctlgrs876660797
Max Magnitude0
ClinVar
Risk rs876660797(T;T)
Alt rs876660797(T;T)
Reference rs876660797(C;C)
Significance 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.131939068C>T
CLNSRC
CLNACC RCV000215726.1,