Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10491363 1.000 0.040 5 100632674 intergenic variant C/T snv 7.3E-02 1
rs80338880 0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs12712079 1.000 0.040 2 100642838 non coding transcript exon variant C/G;T snv 1
rs282072 1.000 0.040 5 100642934 regulatory region variant A/C snv 0.58 1
rs11695640 1.000 0.040 2 100647945 intron variant A/C;T snv 1
rs10153955 1.000 0.040 2 100648418 intron variant A/G snv 0.34 1
rs6743494 1.000 0.040 2 100657433 upstream gene variant T/C snv 0.67 1
rs4850942 1.000 0.040 2 100658375 upstream gene variant A/C snv 0.66 1
rs16898690 1.000 0.040 8 100673904 regulatory region variant G/A;C snv 1
rs2978125 1.000 0.040 8 100676883 regulatory region variant G/A snv 6.3E-03 1
rs1786330 1.000 0.040 8 100679902 upstream gene variant C/T snv 0.28 1
rs1786329 1.000 0.040 8 100680650 upstream gene variant C/A;T snv 1
rs6995748 1.000 0.040 8 100697855 intron variant T/C snv 4.6E-02 1
rs1786322 1.000 0.040 8 100699925 intron variant A/C snv 0.57 1
rs1693552 1.000 0.040 8 100705461 intron variant A/G snv 0.28 1
rs3133575 1.000 0.040 8 100713023 intron variant G/C snv 0.18 1
rs2132853 1.000 0.040 8 100720120 intron variant T/G snv 0.19 1
rs1965214 1.000 0.040 3 100992426 intron variant T/C snv 0.17 1
rs2713758 1.000 0.040 3 100992739 intron variant G/A snv 0.84 1
rs1449305 1.000 0.040 3 100994283 upstream gene variant G/A snv 0.16 1
rs16843128 1.000 0.040 3 100994570 upstream gene variant C/T snv 2.9E-02 1
rs4928102 1.000 0.040 3 100996732 upstream gene variant C/A snv 0.17 1
rs10936464 1.000 0.040 3 100997110 upstream gene variant C/T snv 0.17 1
rs2713798 1.000 0.040 3 100997573 upstream gene variant A/G snv 0.84 1
rs2595907 1.000 0.040 3 100998306 upstream gene variant T/A;C snv 1