rs1319501, NAMPT

N. diseases: 4
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.
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 0.020 1.000 2 2015 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 0.010 1.000 1 2015 2015
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 0.010 1.000 1 2015 2015