Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14