Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs704010 0.851 0.080 10 79081391 intron variant T/C snv 0.71 1
rs1268974 1.000 0.080 10 79092621 intron variant A/G snv 0.65 1
rs1250573 0.827 0.120 10 79282718 intron variant G/A snv 0.23 5
rs12571751 0.925 0.120 10 79182874 intron variant A/G snv 0.46 1
rs10128264 1.000 0.120 10 79200216 intron variant T/C snv 0.64 1
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 1
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs1250550 0.851 0.240 10 79300560 intron variant C/A snv 0.27 5