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rs1839158

From SNPedia

Orientationminus
Stabilizedminus
Make rs1839158(C;C)
Make rs1839158(C;G)
Make rs1839158(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position33630364
is asnp
is mentioned by
dbSNPrs1839158
ebirs1839158
HLIrs1839158
Exacrs1839158
Varsomers1839158
Maprs1839158
PheGenIrs1839158
hapmaprs1839158
1000 genomesrs1839158
hgdprs1839158
ensemblrs1839158
gopubmedrs1839158
geneviewrs1839158
scholarrs1839158
googlers1839158
pharmgkbrs1839158
gwascentralrs1839158
openSNPrs1839158
23andMers1839158
23andMe allrs1839158
SNP Nexus

SNPshotrs1839158
SNPdbers1839158
MSV3drs1839158
GWAS Ctlgrs1839158
GMAF0.3774
Max Magnitude
? (C;C) (C;G) (G;G) 28
GET Evidence
rs1839158
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.296875
summary