rs7865618, CDKN2B-AS1

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.820 1.000 3 2011 2017
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
236 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.800 1.000 2 2012 2012
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.700 1.000 2 2011 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2007 2007
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2012 2012
Arteriovenous hemangioma
CUI: C0334533
Disease: Arteriovenous hemangioma
14 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2014 2014
Congenital arteriovenous malformation
23 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2014 2014
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2011 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2011 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2011 2011
Seizures
CUI: C0036572
Disease: Seizures
553 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2014 2014