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rs876347

From SNPedia

Orientationplus
Stabilizedplus
Make rs876347(A;A)
Make rs876347(A;G)
Make rs876347(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position118268751
is asnp
is mentioned by
dbSNPrs876347
ebirs876347
HLIrs876347
Exacrs876347
Varsomers876347
Maprs876347
PheGenIrs876347
hapmaprs876347
1000 genomesrs876347
hgdprs876347
ensemblrs876347
gopubmedrs876347
geneviewrs876347
scholarrs876347
googlers876347
pharmgkbrs876347
gwascentralrs876347
openSNPrs876347
23andMers876347
23andMe allrs876347
SNP Nexus

SNPshotrs876347
SNPdbers876347
MSV3drs876347
GWAS Ctlgrs876347
GMAF0.1951
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
rs876347
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary