Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 39
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 20
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 18
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 17
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 12
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12