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rs17169056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17169056(A;G)
Make rs17169056(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position15751201
is asnp
is mentioned by
dbSNPrs17169056
ebirs17169056
HLIrs17169056
Exacrs17169056
Varsomers17169056
Maprs17169056
PheGenIrs17169056
hapmaprs17169056
1000 genomesrs17169056
hgdprs17169056
ensemblrs17169056
gopubmedrs17169056
geneviewrs17169056
scholarrs17169056
googlers17169056
pharmgkbrs17169056
gwascentralrs17169056
openSNPrs17169056
23andMers17169056
23andMe allrs17169056
SNP Nexus

SNPshotrs17169056
SNPdbers17169056
MSV3drs17169056
GWAS Ctlgrs17169056
GMAF0.08173
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs17169056
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.046875
summary