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
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
rs2106261 0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs3861950 0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs4076317 0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs4821480 0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs4862423 0.882 0.080 4 184805394 intron variant C/T snv 0.37 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
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
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
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 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
rs1298417395 0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1440763451 0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41