Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs6746030 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs121913474 0.790 0.200 10 121515260 missense variant A/G snv 9
rs16901946 0.827 0.160 8 127088680 non coding transcript exon variant A/G snv 1.7E-02 8
rs2073711 0.807 0.160 15 65201874 missense variant A/G snv 0.56 0.61 7
rs5030772 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs121918505 0.851 0.080 10 121520119 missense variant A/G snv 5
rs904571820 0.851 0.160 6 151842664 start lost A/G snv 4.0E-06 5
rs10948172 0.882 0.040 6 44809954 intron variant A/G snv 0.27 3
rs12901071 0.882 0.160 15 67078051 intron variant A/G snv 0.25 3
rs1800802 0.925 0.040 12 14885985 intron variant A/G snv 0.15 3
rs226794 0.882 0.160 21 26930036 missense variant A/G snv 0.83 0.89 3
rs1044122 0.925 0.040 10 126036209 synonymous variant A/G snv 0.27 0.26 2
rs11564299 0.925 0.040 18 28180064 upstream gene variant A/G snv 0.17 2
rs13301537 0.925 0.040 9 92466765 intron variant A/G snv 0.38 2
rs1913707 0.925 0.040 4 13037816 intergenic variant A/G snv 0.40 2
rs3771501 0.925 0.040 2 70490521 intron variant A/G snv 0.60 2
rs520540 0.925 0.120 11 102838694 synonymous variant A/G snv 0.57 0.54 2
rs835487 0.925 0.040 12 104666989 intron variant A/G snv 0.43 2
rs912428 0.925 0.040 13 46593768 intron variant A/G snv 0.84 2
rs116855380 1.000 0.040 20 47491550 downstream gene variant A/G snv 2.8E-02 1
rs11688000 1.000 0.040 2 75066030 intron variant A/G snv 0.34 1
rs11842874 1.000 0.040 13 113040195 intron variant A/G snv 0.12 1