Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1021479 16 85923808 upstream gene variant T/A;C snv 2
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 2
rs10489481 1 185422035 regulatory region variant G/A snv 0.31 2
rs10987830 9 128016459 intergenic variant G/A snv 6.8E-03 2
rs112313229 3 46323369 intergenic variant G/A;T snv 2
rs112721625 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 2
rs11640143 16 85955858 regulatory region variant T/C;G snv 2
rs11686139 2 226426699 intergenic variant A/C snv 0.13 2
rs117424492 15 79975053 upstream gene variant G/C;T snv 2
rs11775706 8 6843366 intron variant C/G;T snv 2
rs11992162 8 11979005 upstream gene variant G/A;C;T snv 2
rs12149363 16 85895099 upstream gene variant C/G snv 7.9E-02 2
rs12232384 16 85976154 intron variant C/A;T snv 2
rs12898000 14 103368791 upstream gene variant G/C;T snv 2
rs12916091 15 79930230 downstream gene variant T/G snv 0.53 2
rs12973608 19 18287220 upstream gene variant A/C;G snv 2
rs13022141 2 136131638 intergenic variant A/G snv 0.69 2
rs140058837 3 46313128 upstream gene variant A/G snv 2.2E-02 2
rs1400745 14 34886094 intergenic variant A/G snv 0.41 2
rs142105922 16 85968988 intron variant TAATAA/-;TAA;TAATAATAA;TAATAATAATAA;TAATAATAATAATAA delins 2
rs144110170 11 122649353 regulatory region variant C/- delins 0.13 2
rs146723115 8 67901594 intergenic variant AT/-;ATAT;ATATAT;ATATTTATATATAATATATATAATTTATATATATATATATAT delins 2
rs150861794 13 108351457 intron variant C/T snv 1.7E-02 2
rs199741557 4 104943373 intron variant TC/- delins 2.6E-02 2
rs200516372 3 141484141 upstream gene variant A/G snv 2.4E-02 2