Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs3749474 0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs2075685 0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10