Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs363371 0.882 0.120 10 117226885 TF binding site variant G/A snv 0.19 5
rs4911414 0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73 5
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs2395163 0.882 0.160 6 32420032 intergenic variant T/C snv 0.17 3
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs823118 0.925 0.080 1 205754444 upstream gene variant C/A;T snv 3
rs10746953 0.925 0.040 9 74302924 regulatory region variant C/T snv 0.44 2
rs12069733 1.000 0.040 1 43475837 TF binding site variant G/A snv 0.37 2
rs13227860 1.000 0.040 7 22114836 downstream gene variant G/A snv 0.26 2
rs1879553 0.925 0.040 3 118896616 downstream gene variant A/G snv 7.3E-02 2
rs35749011 0.925 0.080 1 155162560 intergenic variant G/A snv 1.1E-02 2
rs363324 0.925 0.120 10 117229651 intergenic variant G/A snv 0.57 2
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