Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs649529 1.000 0.040 11 88275083 intergenic variant G/A;T snv 2
rs6688849 1.000 0.040 1 47530532 intergenic variant A/C;G snv 2
rs6706313 1.000 0.040 2 60311754 regulatory region variant A/G snv 0.18 2
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs1285524167
ABCC8
0.807 0.280 11 17475004 missense variant C/T snv 8.0E-06 8
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 6
rs1272388614
ABCC8
0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs1799854
ABCC8
0.925 0.080 11 17427157 splice region variant G/A snv 0.44 0.37 3
rs28938469
ABCC8
0.925 0.160 11 17395659 missense variant G/A snv 3
rs148529020
ABCC8
1.000 0.040 11 17460613 missense variant C/T snv 1.2E-05 1.4E-05 2
rs756823374
ABCC8
1.000 0.040 11 17463515 missense variant G/A snv 1.4E-05 2
rs2199936
ABCG2
0.882 0.160 4 88124179 intron variant A/G;T snv 0.88 5
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs2239607
ACACB
0.925 0.120 12 109209475 intron variant A/G snv 0.14 3
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv 5
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs735949
ACSL1
0.925 0.080 4 184795078 intron variant T/C snv 0.10 3
rs28647808
ADAMTS13
0.882 0.160 9 133440409 missense variant C/G snv 6.1E-02 5.8E-02 4
rs4607103
ADAMTS9-AS2
0.882 0.120 3 64726228 intron variant C/T snv 0.28 4
rs181914721
ADAMTSL3
1.000 0.040 15 83819856 missense variant G/A snv 3.7E-04 1.2E-04 2