Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs3115573 1.000 0.120 6 32251066 upstream gene variant A/G snv 0.41 2
rs6610650 1.000 0.040 X 37777261 intron variant G/A snv 0.27 2
rs9275424 6 32702799 downstream gene variant A/G snv 0.30 1
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
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
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs4293
ACE
17 63478305 non coding transcript exon variant G/A snv 0.45 1
rs9896208
ACE
17 63498748 intron variant T/C snv 0.57 1
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs11122576
AGT
1.000 0.080 1 230710933 intron variant T/C snv 8.2E-02 2
rs1926723
AGT
1.000 0.080 1 230704350 intron variant T/A;C;G snv 1.2E-05; 0.11; 2.0E-05 2
rs11568054
AGT
1 230709809 intron variant G/A snv 3.6E-02 1