Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659132

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659132(G;T)
Make rs876659132(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132589751
GeneRAD50
is asnp
is mentioned by
dbSNPrs876659132
ebirs876659132
HLIrs876659132
Exacrs876659132
Varsomers876659132
Maprs876659132
PheGenIrs876659132
hapmaprs876659132
1000 genomesrs876659132
hgdprs876659132
ensemblrs876659132
gopubmedrs876659132
geneviewrs876659132
scholarrs876659132
googlers876659132
pharmgkbrs876659132
gwascentralrs876659132
openSNPrs876659132
23andMers876659132
23andMe allrs876659132
SNP Nexus

SNPshotrs876659132
SNPdbers876659132
MSV3drs876659132
GWAS Ctlgrs876659132
Max Magnitude0
ClinVar
Risk rs876659132(T;T)
Alt rs876659132(T;T)
Reference rs876659132(G;G)
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.131925443G>T
CLNSRC
CLNACC RCV000223373.1,