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rs876658770

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658770(C;T)
Make rs876658770(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132640768
GeneRAD50, TH2LCRR
is asnp
is mentioned by
dbSNPrs876658770
ebirs876658770
HLIrs876658770
Exacrs876658770
Varsomers876658770
Maprs876658770
PheGenIrs876658770
hapmaprs876658770
1000 genomesrs876658770
hgdprs876658770
ensemblrs876658770
gopubmedrs876658770
geneviewrs876658770
scholarrs876658770
googlers876658770
pharmgkbrs876658770
gwascentralrs876658770
openSNPrs876658770
23andMers876658770
23andMe allrs876658770
SNP Nexus

SNPshotrs876658770
SNPdbers876658770
MSV3drs876658770
GWAS Ctlgrs876658770
Max Magnitude0
ClinVar
Risk rs876658770(T;T)
Alt rs876658770(T;T)
Reference rs876658770(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene LOC101927761 TH2LCRR RAD50
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131976460C>T
CLNSRC
CLNACC RCV000222314.1,