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rs9533089

From SNPedia

Orientationplus
Stabilizedplus
Make rs9533089(A;A)
Make rs9533089(A;T)
Make rs9533089(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position42376876
is asnp
is mentioned by
dbSNPrs9533089
ebirs9533089
HLIrs9533089
Exacrs9533089
Varsomers9533089
Maprs9533089
PheGenIrs9533089
hapmaprs9533089
1000 genomesrs9533089
hgdprs9533089
ensemblrs9533089
gopubmedrs9533089
geneviewrs9533089
scholarrs9533089
googlers9533089
pharmgkbrs9533089
gwascentralrs9533089
openSNPrs9533089
23andMers9533089
23andMe allrs9533089
SNP Nexus

SNPshotrs9533089
SNPdbers9533089
MSV3drs9533089
GWAS Ctlgrs9533089
GMAF0.2778
Max Magnitude
? (A;A) (A;T) (T;T) 28


GET Evidence
rs9533089
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.241935
summary