Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10011007 4 130143535 intergenic variant A/C snv 8.3E-02 1
rs10031823 4 102203874 intergenic variant T/C snv 0.68 1
rs10044158 5 63666886 intergenic variant G/A snv 0.55 1
rs10175405 2 100703250 regulatory region variant G/T snv 0.33 1
rs10185725 2 154607197 intergenic variant C/T snv 0.35 1
rs10211032 2 116565497 intergenic variant G/A snv 0.47 1
rs10247993 7 127440323 intergenic variant C/T snv 0.66 1
rs1028045 2 100704613 intergenic variant G/A snv 0.38 1
rs10493450 1 68807756 intron variant A/T snv 0.13 1
rs10515007 17 52318179 intergenic variant C/T snv 0.13 1
rs10733389 9 23378222 intron variant A/C;G;T snv 1
rs10736180 10 105603830 intergenic variant G/A snv 0.50 1
rs10757416 9 23344739 intron variant C/T snv 0.35 1
rs1078141 8 141609293 intron variant C/T snv 0.27 1
rs10789907 11 112689091 intron variant A/C snv 0.54 1
rs10804681 3 141941833 upstream gene variant A/T snv 0.88 1
rs10807603 6 16972744 regulatory region variant A/G snv 0.56 1
rs10854884 22 50663471 intergenic variant C/A snv 0.41 1
rs10916805 1 20492166 regulatory region variant G/C snv 0.13 1
rs10930011 2 161045556 downstream gene variant T/A;G snv 1
rs10950995 7 24135246 downstream gene variant T/C snv 0.39 1
rs10954160 7 127564011 intergenic variant A/G;T snv 1
rs10965787 9 23345909 intron variant A/G snv 0.17 1
rs10965796 9 23357495 intron variant A/C;T snv 1
rs10965816 9 23388825 intron variant G/C snv 0.26 1