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rs7672947

From SNPedia

Orientationplus
Stabilizedplus
Make rs7672947(C;C)
Make rs7672947(C;G)
Make rs7672947(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position9959744
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs7672947
ebirs7672947
HLIrs7672947
Exacrs7672947
Varsomers7672947
Maprs7672947
PheGenIrs7672947
hapmaprs7672947
1000 genomesrs7672947
hgdprs7672947
ensemblrs7672947
gopubmedrs7672947
geneviewrs7672947
scholarrs7672947
googlers7672947
pharmgkbrs7672947
gwascentralrs7672947
openSNPrs7672947
23andMers7672947
23andMe allrs7672947
SNP Nexus

SNPshotrs7672947
SNPdbers7672947
MSV3drs7672947
GWAS Ctlgrs7672947
GMAF0.4004
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs7672947
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.421875
summary