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rs1247118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1247118(C;T)
Make rs1247118(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position118669247
is asnp
is mentioned by
dbSNPrs1247118
ebirs1247118
HLIrs1247118
Exacrs1247118
Varsomers1247118
Maprs1247118
PheGenIrs1247118
hapmaprs1247118
1000 genomesrs1247118
hgdprs1247118
ensemblrs1247118
gopubmedrs1247118
geneviewrs1247118
scholarrs1247118
googlers1247118
pharmgkbrs1247118
gwascentralrs1247118
openSNPrs1247118
23andMers1247118
23andMe allrs1247118
SNP Nexus

SNPshotrs1247118
SNPdbers1247118
MSV3drs1247118
GWAS Ctlgrs1247118
GMAF0.2075
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1247118
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.804688
summary