Have questions? Visit https://www.reddit.com/r/SNPedia

rs7676733

From SNPedia

Orientationplus
Stabilizedplus
Make rs7676733(A;A)
Make rs7676733(A;G)
Make rs7676733(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position9965332
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs7676733
ebirs7676733
HLIrs7676733
Exacrs7676733
Varsomers7676733
Maprs7676733
PheGenIrs7676733
hapmaprs7676733
1000 genomesrs7676733
hgdprs7676733
ensemblrs7676733
gopubmedrs7676733
geneviewrs7676733
scholarrs7676733
googlers7676733
pharmgkbrs7676733
gwascentralrs7676733
openSNPrs7676733
23andMers7676733
23andMe allrs7676733
SNP Nexus

SNPshotrs7676733
SNPdbers7676733
MSV3drs7676733
GWAS Ctlgrs7676733
GMAF0.4008
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs7676733
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.421875
summary