Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs6855911 0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs7958822 0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs7131056 0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs2306073 0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs4964057 0.882 0.080 12 27363909 intron variant T/G snv 0.29 3