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rs6449174

From SNPedia

Orientationplus
Stabilizedplus
Make rs6449174(C;C)
Make rs6449174(C;T)
Make rs6449174(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position9964798
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs6449174
ebirs6449174
HLIrs6449174
Exacrs6449174
Varsomers6449174
Maprs6449174
PheGenIrs6449174
hapmaprs6449174
1000 genomesrs6449174
hgdprs6449174
ensemblrs6449174
gopubmedrs6449174
geneviewrs6449174
scholarrs6449174
googlers6449174
pharmgkbrs6449174
gwascentralrs6449174
openSNPrs6449174
23andMers6449174
23andMe allrs6449174
SNP Nexus

SNPshotrs6449174
SNPdbers6449174
MSV3drs6449174
GWAS Ctlgrs6449174
GMAF0.3912
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6449174
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.40625
summary