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

rs7669317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7669317(C;C)
Make rs7669317(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position105536173
is asnp
is mentioned by
dbSNPrs7669317
ebirs7669317
HLIrs7669317
Exacrs7669317
Varsomers7669317
Maprs7669317
PheGenIrs7669317
hapmaprs7669317
1000 genomesrs7669317
hgdprs7669317
ensemblrs7669317
gopubmedrs7669317
geneviewrs7669317
scholarrs7669317
googlers7669317
pharmgkbrs7669317
gwascentralrs7669317
openSNPrs7669317
23andMers7669317
23andMe allrs7669317
SNP Nexus

SNPshotrs7669317
SNPdbers7669317
MSV3drs7669317
GWAS Ctlgrs7669317
GMAF0.01561
Max Magnitude0
? (C;C) (C;T) (T;T) 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 8E-8
Odds Ratio NR NR