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rs4799915

From SNPedia

Orientationplus
Stabilizedplus
Make rs4799915(C;C)
Make rs4799915(C;T)
Make rs4799915(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position37348676
GeneCELF4
is asnp
is mentioned by
dbSNPrs4799915
ebirs4799915
HLIrs4799915
Exacrs4799915
Varsomers4799915
Maprs4799915
PheGenIrs4799915
hapmaprs4799915
1000 genomesrs4799915
hgdprs4799915
ensemblrs4799915
gopubmedrs4799915
geneviewrs4799915
scholarrs4799915
googlers4799915
pharmgkbrs4799915
gwascentralrs4799915
openSNPrs4799915
23andMers4799915
23andMe allrs4799915
SNP Nexus

SNPshotrs4799915
SNPdbers4799915
MSV3drs4799915
GWAS Ctlgrs4799915
GMAF0.4008
Max Magnitude
? (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



GET Evidence
rs4799915
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.554688
summary