rs4799915
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4799915(C;C) |
Make rs4799915(C;T) |
Make rs4799915(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 37348676 |
Gene | CELF4 |
is a | snp |
is | mentioned by |
dbSNP | rs4799915 |
dbSNP (classic) | rs4799915 |
ClinGen | rs4799915 |
ebi | rs4799915 |
HLI | rs4799915 |
Exac | rs4799915 |
Gnomad | rs4799915 |
Varsome | rs4799915 |
LitVar | rs4799915 |
Map | rs4799915 |
PheGenI | rs4799915 |
Biobank | rs4799915 |
1000 genomes | rs4799915 |
hgdp | rs4799915 |
ensembl | rs4799915 |
geneview | rs4799915 |
scholar | rs4799915 |
rs4799915 | |
pharmgkb | rs4799915 |
gwascentral | rs4799915 |
openSNP | rs4799915 |
23andMe | rs4799915 |
SNPshot | rs4799915 |
SNPdbe | rs4799915 |
MSV3d | rs4799915 |
GWAS Ctlg | rs4799915 |
GMAF | 0.4008 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs4799915 |
PubMedID | [PMID 18521091] |
Condition | Response to iloperidone treatment (QT prolongation) |
Gene | BRUNOL4 |
Risk Allele | T |
pValue | 3.00E-006 |
OR | NA |
95% CI |