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rs876658784

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658784(G;T)
Make rs876658784(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132559283
GeneRAD50
is asnp
is mentioned by
dbSNPrs876658784
ebirs876658784
HLIrs876658784
Exacrs876658784
Varsomers876658784
Maprs876658784
PheGenIrs876658784
hapmaprs876658784
1000 genomesrs876658784
hgdprs876658784
ensemblrs876658784
gopubmedrs876658784
geneviewrs876658784
scholarrs876658784
googlers876658784
pharmgkbrs876658784
gwascentralrs876658784
openSNPrs876658784
23andMers876658784
23andMe allrs876658784
SNP Nexus

SNPshotrs876658784
SNPdbers876658784
MSV3drs876658784
GWAS Ctlgrs876658784
Max Magnitude0
ClinVar
Risk rs876658784(T;T)
Alt rs876658784(T;T)
Reference rs876658784(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.131894975G>T
CLNSRC
CLNACC RCV000218272.1,