Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005133 1.000 0.120 22 19750832 intergenic variant C/T snv 0.20 1
rs10097964 1.000 0.120 8 21125392 intron variant G/A snv 2.6E-02 1
rs10175798 1.000 0.120 2 30226728 upstream gene variant G/A snv 0.51 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs10520789 1.000 0.120 15 95598638 regulatory region variant G/A snv 0.12 1
rs10790268 1.000 0.120 11 118858682 intergenic variant A/G;T snv 1
rs11051970 1.000 0.120 12 32384554 downstream gene variant G/T snv 0.33 1
rs11089637 1.000 0.120 22 21624807 downstream gene variant T/C snv 0.28 1
rs11148643 1.000 0.120 13 64317065 intergenic variant T/A;C snv 0.46 1
rs112112734 1.000 0.120 6 32486076 intergenic variant T/C snv 0.37 1
rs11217037 1.000 0.120 11 118806377 intergenic variant G/A snv 0.17 1
rs112300936 1.000 0.120 1 116738074 downstream gene variant C/- del 8.5E-04 1
rs114456288 1.000 0.120 3 86448244 intergenic variant G/A;T snv 1
rs11571302 0.925 0.200 2 203878211 downstream gene variant G/A;T snv 1
rs11599217 1.000 0.120 10 126878395 intergenic variant G/T snv 0.34 1
rs11761231 1.000 0.120 7 131685280 intergenic variant T/C snv 0.66 1
rs11900673 1.000 0.120 2 62225526 downstream gene variant C/T snv 0.13 1
rs11933540 1.000 0.120 4 26118379 downstream gene variant T/C snv 0.37 1
rs12109285 1.000 0.120 5 21749239 intron variant T/A;C snv 1
rs12194148 0.925 0.160 6 32476421 upstream gene variant G/C;T snv 1
rs12519788 1.000 0.120 5 30404961 intergenic variant G/A snv 0.35 1
rs12524487 0.925 0.160 6 31386461 upstream gene variant C/T snv 5.9E-02 1
rs12525220 1.000 0.120 6 32707693 upstream gene variant G/A snv 5.6E-02 1
rs12529514 1.000 0.120 6 14096427 regulatory region variant T/C snv 4.7E-02 1
rs12570744 1.000 0.120 10 6747501 intron variant C/T snv 0.20 1