Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs3844283 0.882 0.200 3 10222796 missense variant C/G snv 0.37 0.35 3
rs708035 0.925 0.120 3 10234479 missense variant T/A snv 0.73 0.70 2
rs7258015 0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs802791 0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs3087456 0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs4774 0.807 0.240 16 10906991 missense variant G/C snv 0.30 0.28 7
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs33996649 0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13