Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs764803020 0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06 5
rs781490101 0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 19
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99