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

rs6449176

From SNPedia

Orientationplus
Stabilizedplus
Make rs6449176(A;A)
Make rs6449176(A;G)
Make rs6449176(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position9966219
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs6449176
ebirs6449176
HLIrs6449176
Exacrs6449176
Varsomers6449176
Maprs6449176
PheGenIrs6449176
hapmaprs6449176
1000 genomesrs6449176
hgdprs6449176
ensemblrs6449176
gopubmedrs6449176
geneviewrs6449176
scholarrs6449176
googlers6449176
pharmgkbrs6449176
gwascentralrs6449176
openSNPrs6449176
23andMers6449176
23andMe allrs6449176
SNP Nexus

SNPshotrs6449176
SNPdbers6449176
MSV3drs6449176
GWAS Ctlgrs6449176
GMAF0.4008
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs6449176
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.421875
summary