Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2144908 0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs2518136 0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs6495446 0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs7895340 0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100