Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs2740488 0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs56131196 0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 6
rs157582 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs2678379 1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs157580 0.882 0.160 19 44892009 intron variant G/A snv 0.69 4
rs261291 1.000 0.080 15 58387979 intron variant T/A;C snv 4
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 3
rs483082 1.000 0.080 19 44912921 non coding transcript exon variant G/T snv 0.28 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3