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rs4837752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4837752(A;A)
Make rs4837752(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position120294359
is asnp
is mentioned by
dbSNPrs4837752
ebirs4837752
HLIrs4837752
Exacrs4837752
Varsomers4837752
Maprs4837752
PheGenIrs4837752
hapmaprs4837752
1000 genomesrs4837752
hgdprs4837752
ensemblrs4837752
gopubmedrs4837752
geneviewrs4837752
scholarrs4837752
googlers4837752
pharmgkbrs4837752
gwascentralrs4837752
openSNPrs4837752
23andMers4837752
23andMe allrs4837752
SNP Nexus

SNPshotrs4837752
SNPdbers4837752
MSV3drs4837752
GWAS Ctlgrs4837752
GMAF0.1717
Max Magnitude0
? (A;A) (A;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 0.000006
Odds Ratio NR NR


GET Evidence
rs4837752
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary