HTR2A, 5-hydroxytryptamine receptor 2A, 3356

N. diseases: 289; N. variants: 34
Disease: Inattention ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7984966
rs7984966
Entrez Id: 3356;100874082
Gene Symbol: HTR2A;HTR2A-AS1
HTR2A;HTR2A-AS1
CUI: C0424101
Disease:
Inattention 		0.010 GeneticVariation BEFREE Mediation analysis suggested that CE (38%) and RTV (44%) substantially mediated the association between inattention and the T-allele of SNP rs3785157 in the norepinephrine transporter gene (SLC6A2) and the T-allele of SNP rs7984966 in HTR2A, respectively. 27230021 2016
dbSNP: rs6313
rs6313
Entrez Id: 3356
Gene Symbol: HTR2A
HTR2A
CUI: C0424101
Disease:
Inattention 		0.010 GeneticVariation BEFREE Furthermore, two candidate genes for ADHD, the COMT VAL158MET and the 5-HT2a T102C polymorphisms, were tested for associations with the ASRS subscales inattention and hyperactivity/impulsivity in N = 203 healthy subjects. 16362639 2006
dbSNP: rs75634836
rs75634836
Entrez Id: 3356
Gene Symbol: HTR2A
HTR2A
CUI: C0424101
Disease:
Inattention 		0.010 GeneticVariation BEFREE Furthermore, two candidate genes for ADHD, the COMT VAL158MET and the 5-HT2a T102C polymorphisms, were tested for associations with the ASRS subscales inattention and hyperactivity/impulsivity in N = 203 healthy subjects. 16362639 2006