Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs6499186 1.000 0.040 16 68626662 downstream gene variant C/T snv 0.84 1
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs887304
CRACR2A
0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2
rs10272006
SP4
0.925 0.080 7 21480514 intron variant G/A snv 0.75 3
rs2668423
PWWP3A
1.000 0.040 19 1370527 intron variant T/G snv 0.73 1
rs2303861
CD82
1.000 0.040 11 44618466 intron variant A/G snv 0.73 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs5748926 1.000 0.040 22 17168884 upstream gene variant T/C snv 0.70 1
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs4844880
HSD11B1-AS1 ; HSD11B1
0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs4783819
FTO
0.925 0.120 16 53782735 intron variant G/C snv 0.68 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62 1
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs1057613
MTTP
1.000 0.040 4 99583828 3 prime UTR variant G/A snv 0.60 1
rs139051
PNPLA3
1.000 0.040 22 43928796 intron variant A/G snv 0.56 0.59 1
rs7946
PEMT
0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 6
rs6993
GOT2
0.925 0.080 16 58707463 3 prime UTR variant A/G snv 0.59 3
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10