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rs9424490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9424490(C;G)
Make rs9424490(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position232886124
GeneLOC101927711
is asnp
is mentioned by
dbSNPrs9424490
ebirs9424490
HLIrs9424490
Exacrs9424490
Varsomers9424490
Maprs9424490
PheGenIrs9424490
hapmaprs9424490
1000 genomesrs9424490
hgdprs9424490
ensemblrs9424490
gopubmedrs9424490
geneviewrs9424490
scholarrs9424490
googlers9424490
pharmgkbrs9424490
gwascentralrs9424490
openSNPrs9424490
23andMers9424490
23andMe allrs9424490
SNP Nexus

SNPshotrs9424490
SNPdbers9424490
MSV3drs9424490
GWAS Ctlgrs9424490
GMAF0.1635
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs9424490
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.203125
summary