Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs3772622 0.851 0.080 3 148717966 intron variant T/A;C snv 4
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306