Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 4
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs35568725
PLIN2
0.925 0.080 9 19119676 missense variant A/G snv 4.1E-02 4.0E-02 3
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs762304200
SHBG
17 7630716 synonymous variant A/G snv 2.8E-05 2
rs771038258
SELENBP1
1 151365837 missense variant A/G snv 8.0E-06 2.1E-05 2
rs1685354
UCP3
11 74002546 intron variant A/G snv 0.30 1
rs217434
NPC1L1
7 44513639 synonymous variant A/G snv 0.16 0.17 1
rs2229268
LRP2
2 169168573 synonymous variant A/G snv 0.20 0.16 1
rs751671151
PLAT
8 42180286 missense variant A/G snv 4.0E-06 1.4E-05 1
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs4646156
ACE2
X 15578920 intron variant A/T snv 2
rs66698963
FADS2
11 61835025 intron variant ACTTCTCCCTGCCTCCCCAGGGACTTCTCCCTGCCTCCCCAGGG/-;ACTTCTCCCTGCCTCCCCAGGG delins 0.56 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs35829419
NLRP3
0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs805297
BAG6 ; APOM
0.851 0.280 6 31654829 intron variant C/A snv 0.23 6
rs3767140
HSPG2
1.000 0.080 1 21888152 intron variant C/A snv 0.25 3
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs12363280
SIRT3
11 231980 intron variant C/A;G snv 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140