Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs10146997 0.827 0.240 14 79478819 intron variant A/G snv 0.25 6