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rs6449171

From SNPedia

Orientationplus
Stabilizedplus
Make rs6449171(C;C)
Make rs6449171(C;T)
Make rs6449171(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position9964374
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs6449171
ebirs6449171
HLIrs6449171
Exacrs6449171
Varsomers6449171
Maprs6449171
PheGenIrs6449171
hapmaprs6449171
1000 genomesrs6449171
hgdprs6449171
ensemblrs6449171
gopubmedrs6449171
geneviewrs6449171
scholarrs6449171
googlers6449171
pharmgkbrs6449171
gwascentralrs6449171
openSNPrs6449171
23andMers6449171
23andMe allrs6449171
SNP Nexus

SNPshotrs6449171
SNPdbers6449171
MSV3drs6449171
GWAS Ctlgrs6449171
GMAF0.3907
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6449171
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.40625
summary