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rs876658976

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658976(-;-)
Make rs876658976(-;T)
Make rs876658976(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132608640
GeneRAD50
is asnp
is mentioned by
dbSNPrs876658976
ebirs876658976
HLIrs876658976
Exacrs876658976
Varsomers876658976
Maprs876658976
PheGenIrs876658976
hapmaprs876658976
1000 genomesrs876658976
hgdprs876658976
ensemblrs876658976
gopubmedrs876658976
geneviewrs876658976
scholarrs876658976
googlers876658976
pharmgkbrs876658976
gwascentralrs876658976
openSNPrs876658976
23andMers876658976
23andMe allrs876658976
SNP Nexus

SNPshotrs876658976
SNPdbers876658976
MSV3drs876658976
GWAS Ctlgrs876658976
Max Magnitude0
ClinVar
Risk rs876658976(T;T)
Alt rs876658976(T;T)
Reference rs876658976(;)
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.131944332dupT
CLNSRC
CLNACC RCV000217594.1,