ITGB3, integrin subunit beta 3, 3690

N. diseases: 260; N. variants: 44
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2317385
rs2317385
Entrez Id: 3690
Gene Symbol: ITGB3
ITGB3
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE Integrin β3 is encoded by the ITGB3 gene, previously identified as a quantitative trait locus (QTL) for 5-HT blood levels in ASD at single nucleotide polymorphism (SNP) rs2317385. 30535103 2019
dbSNP: rs55827077
rs55827077
Entrez Id: 3690
Gene Symbol: ITGB3
ITGB3
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE Our results support rs55827077 as the functional ITGB3 gene promoter variant contributing to elevated 5-HT blood levels in ASD and define a mechanistic chain of events linking ITGB3 to hyperserotonemia. 30535103 2019
dbSNP: rs5918
rs5918
Entrez Id: 3690
Gene Symbol: ITGB3
ITGB3
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE Our studies identify a complex regulation of 5-HT homeostasis and behaviors by integrin αvβ3, revealing an important role for integrins in modulating risk for neuropsychiatric disorders.<b>SIGNIFICANCE STATEMENT</b> The integrin β3 Leu33Pro coding polymorphism has been associated with autism spectrum disorders (ASDs) within a subgroup of patients with elevated blood 5-HT levels, linking integrin β3, 5-HT, and ASD risk. 29038237 2017
dbSNP: rs12603582
rs12603582
Entrez Id: 3690
Gene Symbol: ITGB3
ITGB3
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE Interestingly, rs12603582 is strongly associated with pre-term delivery in our ASD patients (P=0.008). 21102624 2011