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rs2842951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2842951(C;T)
Make rs2842951(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position18135452
GeneTPMT
is asnp
is mentioned by
dbSNPrs2842951
ebirs2842951
HLIrs2842951
Exacrs2842951
Varsomers2842951
Maprs2842951
PheGenIrs2842951
hapmaprs2842951
1000 genomesrs2842951
hgdprs2842951
ensemblrs2842951
gopubmedrs2842951
geneviewrs2842951
scholarrs2842951
googlers2842951
pharmgkbrs2842951
gwascentralrs2842951
openSNPrs2842951
23andMers2842951
23andMe allrs2842951
SNP Nexus

SNPshotrs2842951
SNPdbers2842951
MSV3drs2842951
GWAS Ctlgrs2842951
GMAF0.3163
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2842951
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.579365
summary