Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18