Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10188118 2 653623 intergenic variant C/G snv 0.33 1
rs10198459 2 176408544 intergenic variant T/A;C;G snv 1
rs10438961 18 45199142 intergenic variant T/G snv 0.25 1
rs10901057 9 131370311 upstream gene variant C/A;G snv 1
rs11169926 12 51855003 downstream gene variant C/A snv 0.26 1
rs116183010 4 87547006 intergenic variant G/A snv 1.4E-02 1
rs116379131 5 39961516 intron variant T/A;C snv 1
rs11709625 3 66772733 intergenic variant C/A snv 0.15 1
rs117247077 11 68224525 intergenic variant C/A;T snv 1
rs11730631 4 10291344 downstream gene variant A/C;G snv 1
rs11781985 8 8732273 intron variant T/C snv 0.20 1
rs12228470 12 51866288 intergenic variant C/A snv 0.25 1
rs12368865 12 58028859 intergenic variant A/G snv 5.8E-02 1
rs12472381 2 59094090 intron variant A/G snv 0.55 1
rs12501884 4 9453964 downstream gene variant A/C;T snv 1
rs12808519 11 69785769 intergenic variant A/T snv 5.4E-02 1
rs141990161 1 119400902 intergenic variant T/A;C;G snv 1
rs1440411 4 143237132 intergenic variant C/T snv 0.57 1
rs1457231 2 160245051 intron variant C/T snv 0.67 1
rs145954970 11 64506358 downstream gene variant C/G snv 1.5E-04 1
rs1549287 16 69556463 intergenic variant A/G snv 0.89 1
rs1860904 4 10355824 intergenic variant A/G snv 0.37 1
rs188917216 4 87951768 regulatory region variant A/C snv 5.5E-03 1
rs200113 5 8652758 intergenic variant T/C snv 0.13 1
rs2219647 16 51699494 intergenic variant G/A;T snv 1