Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1764390
LOC105378642 ; GJA4 ; SMIM12
0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs12659
SLC19A1
0.925 0.120 21 45531642 synonymous variant A/G snv 0.58 0.57 2
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs1880669
TF
0.925 0.080 3 133764852 intron variant T/C snv 0.57 0.52 2
rs9574
PROCR ; MMP24-AS1-EDEM2
1.000 0.080 20 35176829 3 prime UTR variant C/A;G;T snv 1.1E-03; 0.55 2
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs2277984
C3
0.925 0.120 19 6679500 splice region variant C/T snv 0.52 0.50 3
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4341
ACE
1.000 0.080 17 63488629 3 prime UTR variant G/C snv 0.50 1
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1062708
MIR6798 ; RUVBL2
1.000 0.080 19 49010016 missense variant C/A;G;T snv 4.3E-06; 1.7E-05; 0.48 1
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs6698843
CELSR2
0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 5
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24