Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10961206 1.000 0.040 9 13724052 intron variant A/T snv 0.12 1
rs11022738 1.000 0.040 11 13271635 regulatory region variant T/C snv 0.32 1
rs11042937 1.000 0.040 11 10723847 upstream gene variant G/T snv 0.59 1
rs111684993 1.000 0.040 15 41144539 intergenic variant A/G snv 0.32 1
rs112009435 1.000 0.040 19 17736035 upstream gene variant G/A;C snv 1
rs11204892 1.000 0.040 1 151795572 upstream gene variant A/G;T snv 1
rs11238907 1.000 0.040 10 44192332 intergenic variant T/G snv 0.25 1
rs113756303 1.000 0.040 8 26245256 intergenic variant G/T snv 0.16 1
rs11610422 1.000 0.040 12 31259735 regulatory region variant A/G snv 0.15 1
rs116161686 1.000 0.040 1 210300277 upstream gene variant G/A snv 9.3E-02 1
rs11677932 1.000 0.040 2 237315312 TF binding site variant G/A snv 0.28 1
rs11723436 1.000 0.040 4 119980181 intergenic variant A/G snv 0.25 1
rs11806316 1.000 0.040 1 115210861 regulatory region variant G/A snv 0.26 1
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 1
rs12219125 0.925 0.120 10 20304158 intergenic variant G/T snv 0.15 1
rs12495221 1.000 0.040 3 48137688 regulatory region variant C/G;T snv 1
rs1254531 1.000 0.040 10 44083614 intergenic variant C/A;T snv 1
rs12619842 1.000 0.040 2 164088534 intron variant G/A;C snv 1
rs12675257 1.000 0.040 8 94267412 intergenic variant C/T snv 0.11 1
rs12788925 1.000 0.040 11 102931118 intergenic variant A/G snv 0.32 1
rs12999907 1.000 0.040 2 164100741 intron variant A/G snv 0.17 1
rs13088645 1.000 0.040 3 134438421 downstream gene variant T/A;G snv 1
rs13102675 1.000 0.040 4 124978810 intergenic variant T/C snv 0.33 1
rs13144478 0.882 0.040 4 115275150 regulatory region variant A/T snv 5.5E-02 1
rs1321309 1.000 0.040 6 36670859 upstream gene variant G/A;C;T snv 0.38 1