Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 5
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs3018362 0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs1564981 16 50952397 intergenic variant G/A snv 0.60 3
rs4580892 6 127088737 intron variant C/T snv 0.32 3
rs6426749 1.000 0.080 1 22384980 intergenic variant G/C snv 0.19 3
rs6532023 1.000 0.080 4 87852697 regulatory region variant T/G snv 0.66 3
rs6913578 0.925 0.080 6 151628671 intergenic variant A/C;T snv 3
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 3
rs1021188 13 42541997 intergenic variant C/T snv 0.79 2
rs10242100 7 121343289 downstream gene variant A/G snv 0.29 2
rs10502386 18 8966146 intergenic variant G/T snv 0.39 2
rs10835187 11 27484130 downstream gene variant C/T snv 0.41 2
rs11755164 6 44671447 regulatory region variant T/C snv 0.57 2
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs12742784 1.000 0.080 1 22355873 intergenic variant C/A;T snv 2
rs12821008 12 49080822 intergenic variant C/T snv 0.30 2
rs13204965 6 126845927 intron variant A/C;T snv 2
rs1346004 2 165744536 downstream gene variant G/A;T snv 2