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

rs17015014

From SNPedia

Orientationplus
Stabilizedplus
Make rs17015014(C;C)
Make rs17015014(C;G)
Make rs17015014(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position141807619
is asnp
is mentioned by
dbSNPrs17015014
ebirs17015014
HLIrs17015014
Exacrs17015014
Varsomers17015014
Maprs17015014
PheGenIrs17015014
hapmaprs17015014
1000 genomesrs17015014
hgdprs17015014
ensemblrs17015014
gopubmedrs17015014
geneviewrs17015014
scholarrs17015014
googlers17015014
pharmgkbrs17015014
gwascentralrs17015014
openSNPrs17015014
23andMers17015014
23andMe allrs17015014
SNP Nexus

SNPshotrs17015014
SNPdbers17015014
MSV3drs17015014
GWAS Ctlgrs17015014
GMAF0.2686
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs17015014
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.21875
summary