Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62117160 0.925 0.120 19 44728895 upstream gene variant G/A;T snv 3
rs712484 0.882 0.160 14 48081576 intergenic variant C/A snv 0.14 3
rs7124842 0.882 0.160 11 76600576 intergenic variant G/A;C;T snv 3
rs7713145 1.000 0.040 5 177354208 upstream gene variant G/A snv 0.37 3
rs878860 0.882 0.120 11 7946812 intergenic variant C/T snv 0.35 3
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 2
rs11242709 1.000 0.040 6 209159 upstream gene variant C/T snv 0.19 2
rs11255753 1.000 0.040 10 8563590 intergenic variant G/C;T snv 0.23 2
rs2164983 0.925 0.120 19 8679120 downstream gene variant C/A;G snv 0.19 2
rs224108 0.925 0.120 10 62789851 intron variant T/C;G snv 0.21 2
rs2744939 1.000 0.040 6 34580429 upstream gene variant T/A snv 0.17 2
rs4939490 0.925 0.120 11 61026179 intergenic variant C/G snv 0.39 2
rs519973 1.000 0.040 3 187915480 intergenic variant G/A snv 0.33 2
rs5743399 0.925 0.120 8 6880123 intron variant G/A snv 0.31 2
rs61192126 1.000 0.040 3 72345701 intergenic variant T/C snv 0.26 2
rs6473227 0.925 0.120 8 80373657 intron variant C/A snv 0.54 2
rs76167968 1.000 0.040 1 35216137 intergenic variant T/C snv 0.25 2
rs10131567 1.000 0.040 14 35395672 intergenic variant G/T snv 0.22 1
rs10244416 1.000 0.040 7 20536128 intergenic variant C/A;T snv 0.52 1
rs10468514 1.000 0.040 17 45378874 intergenic variant A/G snv 0.38 1
rs10489854 1.000 0.040 1 159279069 non coding transcript exon variant C/T snv 8.3E-02 1
rs111267073 1.000 0.040 5 111030094 intergenic variant C/T snv 1.9E-02 1
rs11213941 1.000 0.040 11 111563369 downstream gene variant T/C snv 0.35 1
rs114997373 1.000 0.040 1 45535906 downstream gene variant G/A snv 1.2E-02 1
rs118013485 1.000 0.040 19 33235671 TF binding site variant G/A snv 5.0E-02 1