Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18