CPLX2, complexin 2, 10814

N. diseases: 22; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2434237
rs2434237 		1.000 0.080 5 175797902 intron variant C/A snv 0.18
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs55914911
rs55914911 		5 175817434 intron variant A/G snv 8.9E-02
CUI: C1832423
Disease: Cataract, Age-Related Nuclear
Cataract, Age-Related Nuclear 		Eye Diseases 0.700 1.000 1 2014 2014
dbSNP: rs7448069
rs7448069 		1.000 0.040 5 175817031 intron variant C/A;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2013 2013