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rs1158392

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1158392(C;T)
Make rs1158392(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position75483619
is asnp
is mentioned by
dbSNPrs1158392
ebirs1158392
HLIrs1158392
Exacrs1158392
Varsomers1158392
Maprs1158392
PheGenIrs1158392
hapmaprs1158392
1000 genomesrs1158392
hgdprs1158392
ensemblrs1158392
gopubmedrs1158392
geneviewrs1158392
scholarrs1158392
googlers1158392
pharmgkbrs1158392
gwascentralrs1158392
openSNPrs1158392
23andMers1158392
23andMe allrs1158392
SNP Nexus

SNPshotrs1158392
SNPdbers1158392
MSV3drs1158392
GWAS Ctlgrs1158392
GMAF0.2938
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1158392
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.226562
summary