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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
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
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
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
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs174577 1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs711752 1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs11613352 0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs174556 0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs2144300 0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs2131925 1 62560271 intron variant G/T snv 0.57 6