Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs312053 2 21205177 intergenic variant A/C snv 0.35 1
rs313021 18 1883793 non coding transcript exon variant G/A snv 0.56 1
rs34681481 5 3704137 intergenic variant A/G snv 0.26 1
rs35429 12 115118062 intergenic variant A/G;T snv 1
rs36037977 20 4445885 regulatory region variant G/A snv 5.9E-02 1
rs448385 1 25068642 intron variant G/A snv 0.41 1
rs4682671 3 134274473 intergenic variant T/C;G snv 1
rs4911250 20 32629151 downstream gene variant T/A snv 0.19 1
rs607342 6 139509081 intron variant A/C snv 0.53 1
rs6679817 1 88897581 intergenic variant C/T snv 0.25 1
rs6683021 1 232394844 downstream gene variant A/G snv 0.30 1
rs67385572 2 28424836 upstream gene variant A/G snv 0.13 1
rs6800730 3 48132720 intergenic variant A/G snv 0.64 1
rs68085814 17 49058513 downstream gene variant G/A snv 0.28 1
rs72810955 5 173870299 intergenic variant C/T snv 0.25 1
rs72915163 18 51266459 regulatory region variant C/G;T snv 1
rs74966104 11 55100378 intergenic variant A/G snv 8.4E-02 1
rs7721613 5 68403865 intergenic variant A/G snv 0.37 1
rs7763350 6 43381570 intron variant A/C;G snv 0.44 1
rs782520 7 134509749 regulatory region variant A/G snv 0.57 1
rs78299715 8 20048393 intergenic variant C/G snv 6.1E-02 1
rs7841408 8 128400582 downstream gene variant A/G snv 0.39 1
rs9291932 5 68747416 intergenic variant T/C snv 0.22 1
rs9317097 13 22596235 upstream gene variant C/T snv 0.80 1
rs9603502 13 31671676 intergenic variant C/A snv 0.32 1