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rs17295389

From SNPedia

Orientationplus
Stabilizedplus
Make rs17295389(A;A)
Make rs17295389(A;G)
Make rs17295389(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position81741664
is asnp
is mentioned by
dbSNPrs17295389
ebirs17295389
HLIrs17295389
Exacrs17295389
Varsomers17295389
Maprs17295389
PheGenIrs17295389
hapmaprs17295389
1000 genomesrs17295389
hgdprs17295389
ensemblrs17295389
gopubmedrs17295389
geneviewrs17295389
scholarrs17295389
googlers17295389
pharmgkbrs17295389
gwascentralrs17295389
openSNPrs17295389
23andMers17295389
23andMe allrs17295389
SNP Nexus

SNPshotrs17295389
SNPdbers17295389
MSV3drs17295389
GWAS Ctlgrs17295389
GMAF0.0551
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs17295389
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0546875
summary