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
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 5
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 5
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 2
rs275645 3 148746667 downstream gene variant G/A snv 0.43 1
rs137852671 0.790 0.160 11 17394295 missense variant C/T snv 10
rs909221872 1 6349856 missense variant G/T snv 1
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs3750625 10 111079843 3 prime UTR variant C/A snv 8.7E-02 2