Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10431335 1.000 0.040 12 128194523 upstream gene variant C/A;T snv 1
rs10847434 1.000 0.040 12 127676248 intergenic variant C/T snv 0.29 1
rs10858300 1.000 0.040 9 134950654 intergenic variant C/T snv 0.24 1
rs11753872 1.000 0.040 6 29769165 intergenic variant C/A snv 8.0E-02 1
rs11785210 1.000 0.040 8 15795369 intergenic variant T/C snv 1.4E-02 1
rs11924705 1.000 0.040 3 162443828 intergenic variant T/C snv 0.33 1
rs12091564 1.000 0.040 1 146039391 upstream gene variant A/C;G snv 1
rs12200560 1.000 0.040 6 96632322 intergenic variant A/G snv 0.36 1
rs12210887 1.000 0.040 6 31847946 intergenic variant G/T snv 9.5E-02 1
rs12211490 1.000 0.040 6 33757751 intergenic variant G/T snv 0.12 1
rs12227162 1.000 0.040 12 110929440 intergenic variant C/G;T snv 4.6E-03 1
rs12638067 1.000 0.040 3 187674130 upstream gene variant T/C snv 0.11 1
rs12646936 1.000 0.040 4 135841484 intergenic variant T/G snv 0.59 1
rs12829757 1.000 0.040 12 128176746 intergenic variant G/C snv 0.50 1
rs13232179 1.000 0.040 7 151423862 upstream gene variant T/A;C snv 0.13 1
rs1362076 1.000 0.040 6 29473392 upstream gene variant G/A;T snv 1
rs1395821 1.000 0.040 4 147126398 intron variant C/T snv 0.70 1
rs1400558 1.000 0.040 4 147459653 upstream gene variant T/C snv 0.64 1
rs1471678 1.000 0.040 8 62183763 intergenic variant C/A;T snv 1
rs1614866 1.000 0.040 1 211527316 regulatory region variant G/A snv 7.1E-02 1
rs16867808 1.000 0.040 6 27495905 intron variant T/C snv 6.6E-02 1
rs1842896 1.000 0.040 4 155590307 intergenic variant G/T snv 0.50 1
rs1943950 1.000 0.040 21 30107534 intergenic variant G/A;T snv 1
rs2064092 1.000 0.040 6 27543592 intergenic variant C/A snv 0.13 1
rs2123536 1.000 0.040 2 19745816 intergenic variant T/A;C snv 1