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

rs17022444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17022444(C;G)
Make rs17022444(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position82802345
is asnp
is mentioned by
dbSNPrs17022444
ebirs17022444
HLIrs17022444
Exacrs17022444
Varsomers17022444
Maprs17022444
PheGenIrs17022444
hapmaprs17022444
1000 genomesrs17022444
hgdprs17022444
ensemblrs17022444
gopubmedrs17022444
geneviewrs17022444
scholarrs17022444
googlers17022444
pharmgkbrs17022444
gwascentralrs17022444
openSNPrs17022444
23andMers17022444
23andMe allrs17022444
SNP Nexus

SNPshotrs17022444
SNPdbers17022444
MSV3drs17022444
GWAS Ctlgrs17022444
GMAF0.01331
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19875103OA-icon.png]
Trait Response to antipsychotic therapy (extrapyramidal side effects)
Title Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects
Risk Allele
P-val 1E-10
Odds Ratio NR NR


GET Evidence
rs17022444
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.046875
summary