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rs9345389

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs9345389(A;G)
Make rs9345389(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position93730886
GeneGNL1
is asnp
is mentioned by
dbSNPrs9345389
ebirs9345389
HLIrs9345389
Exacrs9345389
Varsomers9345389
Maprs9345389
PheGenIrs9345389
hapmaprs9345389
1000 genomesrs9345389
hgdprs9345389
ensemblrs9345389
gopubmedrs9345389
geneviewrs9345389
scholarrs9345389
googlers9345389
pharmgkbrs9345389
gwascentralrs9345389
openSNPrs9345389
23andMers9345389
23andMe allrs9345389
SNP Nexus

SNPshotrs9345389
SNPdbers9345389
MSV3drs9345389
GWAS Ctlgrs9345389
GMAF0.118
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs9345389
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0873016
summary