Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115689251 1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs6506900 1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs7442201 1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs6754498 1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2891168 0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs4272321 1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs2680830 1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs59811240 1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs6606859 1.000 0.080 15 27032254 intron variant C/A;T snv 2