Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
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
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 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
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
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
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20