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
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs2057768 0.925 0.120 16 27310774 upstream gene variant C/A;G;T snv 4
rs10492367 0.882 0.040 12 27862037 regulatory region variant G/T snv 0.12 3
rs11564299 0.925 0.040 18 28180064 upstream gene variant A/G snv 0.17 2
rs1913707 0.925 0.040 4 13037816 intergenic variant A/G snv 0.40 2
rs2785988 0.925 0.040 1 219570796 intergenic variant C/A snv 0.23 2
rs4072286 1.000 0.040 8 141726333 regulatory region variant G/A;T snv 2
rs643472 0.925 0.080 8 29296260 intergenic variant C/T snv 0.73 2
rs9350591 0.925 0.040 6 75531811 intergenic variant C/A;T snv 0.12 2
rs10948155 1.000 0.040 6 44720220 intergenic variant T/C snv 0.30 1
rs116855380 1.000 0.040 20 47491550 downstream gene variant A/G snv 2.8E-02 1
rs12154055 1.000 0.040 6 44481960 intergenic variant G/A snv 0.27 1
rs12618428 1.000 0.040 2 150876465 regulatory region variant A/G snv 0.14 1
rs12923310 1.000 0.040 16 9694080 intergenic variant G/T snv 0.32 1
rs150365637 1.000 0.040 8 9222261 intron variant -/T delins 0.13 1
rs1627411 1.000 0.040 14 42702125 intron variant T/C snv 0.75 1
rs330050 1.000 0.040 8 9230169 intron variant G/C;T snv 1
rs35206230 1.000 0.040 15 74805439 downstream gene variant C/T snv 0.43 1
rs4140564 1.000 0.040 1 186755871 intergenic variant G/A snv 0.93 1
rs4764133 1.000 0.040 12 14911429 downstream gene variant C/G;T snv 1
rs4931462 1.000 0.040 12 31225008 TF binding site variant T/G snv 0.65 1
rs6094710 1.000 0.040 20 47466905 intergenic variant G/A snv 5.0E-02 1
rs614332 1.000 0.040 11 93101032 intergenic variant C/T snv 0.62 1
rs6766414 1.000 0.040 3 31446730 intergenic variant T/G snv 0.22 1