Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs1532002 1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs16879003 1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs17214144 1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs2680830 1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs4272321 1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs59490629 1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs59811240 1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 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
rs6898559 1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs72928364 1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs7442201 1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs74570061 1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs75629841 1.000 0.080 8 124714135 intron variant G/A;T snv 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