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rs17054392

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17054392(C;C)
Make rs17054392(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position168609107
GenePALLD
is asnp
is mentioned by
dbSNPrs17054392
ebirs17054392
HLIrs17054392
Exacrs17054392
Varsomers17054392
Maprs17054392
PheGenIrs17054392
hapmaprs17054392
1000 genomesrs17054392
hgdprs17054392
ensemblrs17054392
gopubmedrs17054392
geneviewrs17054392
scholarrs17054392
googlers17054392
pharmgkbrs17054392
gwascentralrs17054392
openSNPrs17054392
23andMers17054392
23andMe allrs17054392
SNP Nexus

SNPshotrs17054392
SNPdbers17054392
MSV3drs17054392
GWAS Ctlgrs17054392
GMAF0.04086
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18521091]
Trait Response to iloperidone treatment (QT prolongation)
Title Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia
Risk Allele C
P-val 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs17054392
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0793651
summary