Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs633389 1.000 0.040 11 116796621 upstream gene variant C/T snv 0.13 4
rs11774572 1.000 0.040 8 11589291 regulatory region variant C/G;T snv 2
rs1263163 11 116802796 intergenic variant G/A snv 0.10 2
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 3
rs4149339
ABCA1
1.000 0.040 9 104782875 3 prime UTR variant G/A snv 0.32 2
rs4743763
ABCA1
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36 2
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs2285666
ACE2
0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23 4
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv 4
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 4
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs4646155
ACE2
0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 3
rs4830542
ACE2
0.925 0.080 X 15558483 downstream gene variant C/G;T snv 3
rs1978124
ACE2
X 15599940 intron variant T/A;C snv 2
rs4646156
ACE2
X 15578920 intron variant A/T snv 2
rs233575
ACE2
X 15564843 intron variant G/A snv 1
rs4646142
ACE2
X 15584941 intron variant G/A;C snv 1