Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs4253778
PPARA
1.000 0.040 22 46234737 intron variant G/C;T snv 3
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs769455
APOE
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs544453230
LDLR
0.882 0.080 19 11110714 missense variant G/A;C snv 2.8E-05; 4.0E-06 6
rs56225452
SLC27A5 ; LOC105372486 ; ZBTB45
0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs730882082
LDLR
0.882 0.080 19 11105315 missense variant G/A;T snv 1.6E-05 5