CPLX2, complexin 2, 10814

N. diseases: 22; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55914911
rs55914911
Entrez Id: 10814
Gene Symbol: CPLX2
CPLX2
CUI: C1832423
Disease:
Cataract, Age-Related Nuclear 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract. 24951543 2014
dbSNP: rs7448069
rs7448069
Entrez Id: 10814
Gene Symbol: CPLX2
CPLX2
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. 23527680 2013
dbSNP: rs2434237
rs2434237
Entrez Id: 10814
Gene Symbol: CPLX2
CPLX2
CUI: C0027051
Disease:
Myocardial Infarction 		0.700 GeneticVariation GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011