Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs7654093 0.882 0.120 4 154623920 upstream gene variant A/T snv 0.27 6
rs113092656 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs1906591 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 5
rs35436 1.000 0.080 12 115116718 intergenic variant C/T snv 0.40 5
rs60942712 0.882 0.120 3 88998609 intergenic variant G/T snv 7.9E-02 5