Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
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
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
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
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
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