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
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs17748 0.827 0.080 11 118657714 3 prime UTR variant C/T snv 0.18 5
rs745542298 0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs769809364 0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs587782144 0.807 0.160 17 7675139 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 8
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs660118 0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6