rs4076317, ANGPTL4

N. diseases: 5
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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.882 0.080 19 8364115 intron variant C/G snv 0.25 0.010 1.000 1 2018 2018
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.882 0.080 19 8364115 intron variant C/G snv 0.25 0.010 1.000 1 2018 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.882 0.080 19 8364115 intron variant C/G snv 0.25 0.010 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.882 0.080 19 8364115 intron variant C/G snv 0.25 0.010 1.000 1 2008 2008
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.882 0.080 19 8364115 intron variant C/G snv 0.25 0.010 1.000 1 2008 2008