Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs7536827 0.925 0.080 1 146037054 upstream gene variant T/A;C;G snv 3
rs2016116 1.000 0.040 18 35414928 intergenic variant A/G snv 6.4E-03 1
rs482843 1.000 0.040 1 70406697 upstream gene variant A/G snv 0.52 1
rs73079108 1.000 0.040 1 207102148 upstream gene variant G/A snv 0.10 1
rs883062 1.000 0.040 1 42144196 downstream gene variant G/A snv 0.42 1
rs9865108
AADACL2-AS1 ; LOC105374159
1.000 0.040 3 151900547 intron variant T/C snv 0.17 1
rs755418013
ACACA
1.000 0.040 17 37130209 missense variant G/A snv 4.0E-06 1
rs758980216
ACACA
1.000 0.040 17 37149965 missense variant G/A snv 1.2E-05 2.8E-05 1
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 7
rs568401628
ACE
0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 4
rs1221928144
ACE
1.000 0.040 17 63477950 missense variant G/A;C snv 8.2E-06 1
rs12720742
ACE
1.000 0.040 17 63496923 missense variant C/G;T snv 2.4E-05; 3.2E-04 1
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
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
rs6632677
ACE2
0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 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