Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 5
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs2741027 1.000 0.040 2 233609365 downstream gene variant G/A snv 0.22 4
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 3
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11