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rs6449178

From SNPedia

Orientationplus
Stabilizedplus
Make rs6449178(C;C)
Make rs6449178(C;T)
Make rs6449178(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position9967060
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs6449178
ebirs6449178
HLIrs6449178
Exacrs6449178
Varsomers6449178
Maprs6449178
PheGenIrs6449178
hapmaprs6449178
1000 genomesrs6449178
hgdprs6449178
ensemblrs6449178
gopubmedrs6449178
geneviewrs6449178
scholarrs6449178
googlers6449178
pharmgkbrs6449178
gwascentralrs6449178
openSNPrs6449178
23andMers6449178
23andMe allrs6449178
SNP Nexus

SNPshotrs6449178
SNPdbers6449178
MSV3drs6449178
GWAS Ctlgrs6449178
GMAF0.3907
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6449178
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.404762
summary