Have questions? Visit https://www.reddit.com/r/SNPedia

rs17099545

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17099545(A;G)
Make rs17099545(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position102761462
GeneLOC100128088
is asnp
is mentioned by
dbSNPrs17099545
ebirs17099545
HLIrs17099545
Exacrs17099545
Varsomers17099545
Maprs17099545
PheGenIrs17099545
hapmaprs17099545
1000 genomesrs17099545
hgdprs17099545
ensemblrs17099545
gopubmedrs17099545
geneviewrs17099545
scholarrs17099545
googlers17099545
pharmgkbrs17099545
gwascentralrs17099545
openSNPrs17099545
23andMers17099545
23andMe allrs17099545
SNP Nexus

SNPshotrs17099545
SNPdbers17099545
MSV3drs17099545
GWAS Ctlgrs17099545
GMAF0.07851
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs17099545
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0703125
summary