Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258 12 111280427 intron variant C/A;T snv 23
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19