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rs6449172

From SNPedia

Orientationplus
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Make rs6449172(A;A)
Make rs6449172(A;T)
Make rs6449172(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position9964412
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs6449172
ebirs6449172
HLIrs6449172
Exacrs6449172
Varsomers6449172
Maprs6449172
PheGenIrs6449172
hapmaprs6449172
1000 genomesrs6449172
hgdprs6449172
ensemblrs6449172
gopubmedrs6449172
geneviewrs6449172
scholarrs6449172
googlers6449172
pharmgkbrs6449172
gwascentralrs6449172
openSNPrs6449172
23andMers6449172
23andMe allrs6449172
SNP Nexus

SNPshotrs6449172
SNPdbers6449172
MSV3drs6449172
GWAS Ctlgrs6449172
GMAF0.4013
Max Magnitude
? (A;A) (A;T) (T;T) 28


GET Evidence
rs6449172
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency
summary