Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs4416670 0.827 0.240 6 43982716 intergenic variant T/C snv 0.45 7
rs10761731 10 63267850 intron variant A/T snv 0.38 6
rs114694170 1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs10761741 1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs2375980 9 2692622 intergenic variant C/G snv 0.51 3
rs4782371 1.000 0.040 16 88502423 intron variant T/A;G snv 3
rs1740073 1.000 0.040 6 43979661 regulatory region variant T/C snv 0.67 2
rs2375981 1.000 0.040 9 2692583 regulatory region variant C/G;T snv 2
rs6479877 10 63118358 intergenic variant C/A;G;T snv 2
rs7767396 6 43959313 intergenic variant A/G snv 0.48 2
rs12199215 6 44059177 non coding transcript exon variant C/T snv 0.25 2
rs7043199 1.000 0.040 9 2621145 intron variant T/A snv 0.18 2
rs2639990 1.000 0.040 18 75203596 intron variant T/C snv 0.12 2
rs10122587 9 2691951 intergenic variant C/G;T snv 1
rs10967470 9 2675698 intergenic variant A/G snv 0.21 1
rs10967492 9 2681175 intergenic variant T/A snv 0.18 1
rs12214617 6 43972186 intergenic variant G/T snv 0.53 1
rs143479231 3 193393005 intergenic variant G/A snv 1.5E-02 1
rs1776717 6 43983599 regulatory region variant G/A;C snv 1
rs34528081 6 43736680 intron variant -/T ins 0.49 1
rs4513773 6 43957789 intergenic variant A/G snv 0.44 1
rs6475920 9 2673933 intergenic variant C/A;G snv 1