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rs12476047

From SNPedia

Orientationplus
Stabilizedplus
Make rs12476047(C;C)
Make rs12476047(C;T)
Make rs12476047(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position163461366
is asnp
is mentioned by
dbSNPrs12476047
ebirs12476047
HLIrs12476047
Exacrs12476047
Varsomers12476047
Maprs12476047
PheGenIrs12476047
hapmaprs12476047
1000 genomesrs12476047
hgdprs12476047
ensemblrs12476047
gopubmedrs12476047
geneviewrs12476047
scholarrs12476047
googlers12476047
pharmgkbrs12476047
gwascentralrs12476047
openSNPrs12476047
23andMers12476047
23andMe allrs12476047
SNP Nexus

SNPshotrs12476047
SNPdbers12476047
MSV3drs12476047
GWAS Ctlgrs12476047
GMAF0.2548
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19680635]
Trait Antipsychotic-induced schizophrenia
Title Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients
Risk Allele C
P-val 0.000003
Odds Ratio 3.21 [1.97-5.25]


GET Evidence
rs12476047
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary