Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs6068816 0.752 0.200 20 54164552 synonymous variant C/T snv 0.12 8.9E-02 12
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11