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rs10811771

From SNPedia

Orientationplus
Stabilizedplus
Make rs10811771(A;A)
Make rs10811771(A;G)
Make rs10811771(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position22770887
GeneLINC01239
is asnp
is mentioned by
dbSNPrs10811771
dbSNP (classic)rs10811771
ClinGenrs10811771
ebirs10811771
HLIrs10811771
Exacrs10811771
Gnomadrs10811771
Varsomers10811771
LitVarrs10811771
Maprs10811771
PheGenIrs10811771
Biobankrs10811771
1000 genomesrs10811771
hgdprs10811771
ensemblrs10811771
geneviewrs10811771
scholarrs10811771
googlers10811771
pharmgkbrs10811771
gwascentralrs10811771
openSNPrs10811771
23andMers10811771
SNPshotrs10811771
SNPdbers10811771
MSV3drs10811771
GWAS Ctlgrs10811771
GMAF0.2658
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 8E-7
Odds Ratio NR NR