Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs4072111 0.716 0.400 15 81285798 missense variant C/T snv 0.17 0.11 16
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
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2275008 0.827 0.080 14 20448090 non coding transcript exon variant T/A;C snv 4.0E-06; 0.26 5