Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs12040333 1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs1440581 1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs16879003 1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 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
rs6506900 1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs6606859 1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs6754498 1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs7442201 1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs75629841 1.000 0.080 8 124714135 intron variant G/A;T snv 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs944801 0.882 0.120 9 22051671 intron variant G/A;C snv 4
rs4272321 1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs115689251 1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs59811240 1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs113533135 1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs1532002 1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2