Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs1250550 0.851 0.240 10 79300560 intron variant C/A snv 0.27 3
rs1250546 0.925 0.080 10 79272775 intron variant A/G snv 0.36 2
rs704010 0.851 0.080 10 79081391 intron variant T/C snv 0.71 1
rs12571751 0.925 0.120 10 79182874 intron variant A/G snv 0.46 1
rs1749824 0.925 0.080 10 79164105 intron variant C/A snv 0.39 1
rs1250542 1.000 0.080 10 79274913 intron variant G/A snv 0.32 1
rs1250544 0.882 0.080 10 79273128 intron variant G/A snv 0.32 1
rs11593576 0.925 0.040 10 79256139 intron variant C/T snv 0.29 1
rs780151 10 79171724 intron variant G/A snv 0.32 1
rs7916441 10 79165820 intron variant G/C snv 0.39 1