Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 19
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 9
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 8
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 8
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 8
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 7
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 7
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 6
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs4848306 0.851 0.120 2 112840530 non coding transcript exon variant G/A snv 0.39 6
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 6
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 4
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs2069521 0.851 0.240 15 74746626 upstream gene variant G/A snv 4.9E-02 4