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rs1459148

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1459148(A;A)
Make rs1459148(A;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position98374106
is asnp
is mentioned by
dbSNPrs1459148
ebirs1459148
HLIrs1459148
Exacrs1459148
Varsomers1459148
Maprs1459148
PheGenIrs1459148
hapmaprs1459148
1000 genomesrs1459148
hgdprs1459148
ensemblrs1459148
gopubmedrs1459148
geneviewrs1459148
scholarrs1459148
googlers1459148
pharmgkbrs1459148
gwascentralrs1459148
openSNPrs1459148
23andMers1459148
23andMe allrs1459148
SNP Nexus

SNPshotrs1459148
SNPdbers1459148
MSV3drs1459148
GWAS Ctlgrs1459148
GMAF0.01286
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 0.000002
Odds Ratio NR NR


GET Evidence
rs1459148
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0078125
summary