Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24