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rs8060598

From SNPedia

Orientationplus
Make rs8060598(C;C)
Make rs8060598(C;T)
Make rs8060598(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position50747891
GeneCYLD
is asnp
is mentioned by
dbSNPrs8060598
ebirs8060598
HLIrs8060598
Exacrs8060598
Varsomers8060598
Maprs8060598
PheGenIrs8060598
hapmaprs8060598
1000 genomesrs8060598
hgdprs8060598
ensemblrs8060598
gopubmedrs8060598
geneviewrs8060598
scholarrs8060598
googlers8060598
pharmgkbrs8060598
gwascentralrs8060598
openSNPrs8060598
23andMers8060598
23andMe allrs8060598
SNP Nexus

SNPshotrs8060598
SNPdbers8060598
MSV3drs8060598
GWAS Ctlgrs8060598
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25642632] Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy.