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rs876658212

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658212(A;G)
Make rs876658212(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132557325
GeneIL5, RAD50
is asnp
is mentioned by
dbSNPrs876658212
ebirs876658212
HLIrs876658212
Exacrs876658212
Varsomers876658212
Maprs876658212
PheGenIrs876658212
hapmaprs876658212
1000 genomesrs876658212
hgdprs876658212
ensemblrs876658212
gopubmedrs876658212
geneviewrs876658212
scholarrs876658212
googlers876658212
pharmgkbrs876658212
gwascentralrs876658212
openSNPrs876658212
23andMers876658212
23andMe allrs876658212
SNP Nexus

SNPshotrs876658212
SNPdbers876658212
MSV3drs876658212
GWAS Ctlgrs876658212
Max Magnitude0
ClinVar
Risk rs876658212(G;G)
Alt rs876658212(G;G)
Reference rs876658212(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD50 IL5
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.131893017A>G
CLNSRC
CLNACC RCV000222879.1,