Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs708494 1.000 0.040 14 52300623 regulatory region variant G/A snv 0.47 2
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35