rs7669317

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs7669317(C;C)

Make rs7669317(C;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

105536173

is a	snp
is	mentioned by
dbSNP	rs7669317
dbSNP (classic)	rs7669317
ClinGen	rs7669317
ebi	rs7669317
HLI	rs7669317
Exac	rs7669317
Gnomad	rs7669317
Varsome	rs7669317
LitVar	rs7669317
Map	rs7669317
PheGenI	rs7669317
Biobank	rs7669317
1000 genomes	rs7669317
hgdp	rs7669317
ensembl	rs7669317
geneview	rs7669317
scholar	rs7669317
google	rs7669317
pharmgkb	rs7669317
gwascentral	rs7669317
openSNP	rs7669317
23andMe	rs7669317
SNPshot	rs7669317
SNPdbe	rs7669317
MSV3d	rs7669317
GWAS Ctlg	rs7669317

GMAF

0.01561

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 19875103]
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