Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39