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rs2126709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2126709(C;T)
Make rs2126709(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position123725219
GeneZNF202
is asnp
is mentioned by
dbSNPrs2126709
ebirs2126709
HLIrs2126709
Exacrs2126709
Varsomers2126709
Maprs2126709
PheGenIrs2126709
hapmaprs2126709
1000 genomesrs2126709
hgdprs2126709
ensemblrs2126709
gopubmedrs2126709
geneviewrs2126709
scholarrs2126709
googlers2126709
pharmgkbrs2126709
gwascentralrs2126709
openSNPrs2126709
23andMers2126709
23andMe allrs2126709
SNP Nexus

SNPshotrs2126709
SNPdbers2126709
MSV3drs2126709
GWAS Ctlgrs2126709
GMAF0.07025
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 4E-7
Odds Ratio NR NR

[PMID 21162693OA-icon.png] Pharmacogenetics and antipsychotics: therapeutic efficacy and side effects prediction.


GET Evidence
rs2126709
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.046875
summary