rs2235312, APLN

N. diseases: 3
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.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.882 0.160 X 129653118 intron variant A/G snv 0.31 0.010 1.000 1 2016 2016
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.882 0.160 X 129653118 intron variant A/G snv 0.31 0.010 1.000 1 2016 2016
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.160 X 129653118 intron variant A/G snv 0.31 0.010 1.000 1 2016 2016