Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10506095 1.000 0.040 12 32647193 downstream gene variant C/T snv 4.4E-02 1
rs10767971 1.000 0.040 11 32874118 regulatory region variant T/C snv 0.64 1
rs11209290 1.000 0.040 1 68405344 intergenic variant G/A snv 6.7E-02 1
rs12063142 1.000 0.040 1 18813023 intergenic variant C/T snv 0.28 1
rs1296028 1.000 0.040 8 11841238 downstream gene variant A/G snv 0.20 1
rs13016703 1.000 0.040 2 168299085 intergenic variant T/G snv 0.18 1
rs1438852 1.000 0.040 2 118838515 upstream gene variant C/T snv 0.52 1
rs144847051 1.000 0.040 12 33148871 intergenic variant G/A snv 9.7E-04 1
rs1468375 1.000 0.040 7 145337519 intergenic variant C/A;T snv 1
rs1504212 1.000 0.040 5 53824125 upstream gene variant C/A snv 0.51 1
rs1524282 1.000 0.040 7 109606047 intergenic variant A/G snv 6.0E-02 1
rs1561244 1.000 0.040 2 72902257 intergenic variant G/A;T snv 1
rs1630500 1.000 0.040 1 154882579 intergenic variant G/A snv 5.0E-02 1
rs1775143 1.000 0.040 1 205786422 downstream gene variant C/T snv 0.63 1
rs188789342 1.000 0.040 10 119612816 intergenic variant C/T snv 1.3E-02 1
rs1955337 1.000 0.040 2 168272635 regulatory region variant G/T snv 0.15 1
rs2046571 1.000 0.040 8 121343472 intergenic variant G/A;C;T snv 1
rs213462 1.000 0.040 X 83449447 intergenic variant A/C snv 0.50 1
rs2338971 1.000 0.040 1 101414449 intergenic variant T/A;C snv 1
rs2921073 1.000 0.040 8 8450133 intergenic variant C/A;G;T snv 1
rs329648 1.000 0.040 11 133895472 downstream gene variant T/C snv 0.55 1
rs601999 1.000 0.040 17 42546140 intron variant T/C snv 0.63 1
rs6416935 1.000 0.040 17 62107553 intergenic variant G/T snv 0.15 1
rs6532194 1.000 0.040 4 89859751 intergenic variant C/G;T snv 1
rs6532197 1.000 0.040 4 89876150 upstream gene variant A/G snv 0.16 1