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rs6743931

From SNPedia

Orientationplus
Stabilizedplus
Make rs6743931(A;A)
Make rs6743931(A;G)
Make rs6743931(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position239496966
is asnp
is mentioned by
dbSNPrs6743931
ebirs6743931
HLIrs6743931
Exacrs6743931
Varsomers6743931
Maprs6743931
PheGenIrs6743931
hapmaprs6743931
1000 genomesrs6743931
hgdprs6743931
ensemblrs6743931
gopubmedrs6743931
geneviewrs6743931
scholarrs6743931
googlers6743931
pharmgkbrs6743931
gwascentralrs6743931
openSNPrs6743931
23andMers6743931
23andMe allrs6743931
SNP Nexus

SNPshotrs6743931
SNPdbers6743931
MSV3drs6743931
GWAS Ctlgrs6743931
GMAF0.1286
Max Magnitude
? (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
rs6743931
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary