Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3771829 0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs1106854 0.827 0.080 2 75050887 intron variant T/C;G snv 5
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs1386483 0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs17110563 0.827 0.080 12 71972526 missense variant C/T snv 1.2E-03 1.1E-03 7
rs1386482 0.827 0.080 12 72018792 intron variant T/G snv 0.52 5
rs1386486 0.827 0.080 12 72018440 intron variant A/G snv 0.53 5
rs2812393 0.807 0.080 1 231777927 intron variant G/C snv 0.61 6
rs766288 0.790 0.080 1 231557942 intron variant G/T snv 0.40 7