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
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 4
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 3
rs206833 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 3
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs499765 0.925 0.160 19 48763133 downstream gene variant C/G snv 0.45 2
rs62141163 1.000 0.040 2 31440248 regulatory region variant G/A snv 7.6E-02 2
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs117542855 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 1
rs1953124 1.000 0.040 13 65771915 regulatory region variant C/A;G;T snv 1
rs222054 1.000 0.040 4 71738582 downstream gene variant C/G snv 0.27 1
rs497408 1.000 0.040 6 23993395 regulatory region variant C/A;T snv 1