Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2494938 0.752 0.240 6 40568389 intron variant G/A snv 0.51 11