Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250567 0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs1250566 10 79286696 intron variant G/A snv 0.24 1
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs2802372 10 79287818 intron variant A/C snv 0.44 1
rs1782645 1.000 0.080 10 79288854 intron variant C/A;T snv 1
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 1
rs1250550 0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs1250557 1.000 0.080 10 79306017 intron variant G/T snv 0.63 1