Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780159 10 79147390 intron variant A/C;G snv 2
rs1250546 0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs1250544 0.882 0.080 10 79273128 intron variant G/A snv 0.32 3
rs703978 1.000 0.080 10 79184390 intron variant C/G;T snv 0.68 3
rs1250573 0.827 0.120 10 79282718 intron variant G/A snv 0.23 5
rs1250550 0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs1250567 0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14