Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 5
rs258
LPL
8 19954741 intron variant G/A;C;T snv 4
rs3758539
FFAR4 ; RBP4
0.925 0.120 10 93601831 intron variant C/T snv 0.13 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
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs9319428
FLT1
0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs10892151
DSCAML1 ; LOC105369515
1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs1746661
FNDC5
0.925 0.080 1 32869438 intron variant G/A;T snv 3
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 3
rs3767140
HSPG2
1.000 0.080 1 21888152 intron variant C/A snv 0.25 3
rs4253778
PPARA
1.000 0.040 22 46234737 intron variant G/C;T snv 3
rs4646155
ACE2
0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 3
rs11066782
KCTD10
1.000 0.040 12 109472747 intron variant C/T snv 0.17 2
rs11613718
KCTD10
1.000 0.040 12 109474527 intron variant C/T snv 0.17 2
rs1978124
ACE2
X 15599940 intron variant T/A;C snv 2
rs2070665
APOA1 ; APOA1-AS
11 116836968 intron variant A/C;G snv 0.85 2
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs4646156
ACE2
X 15578920 intron variant A/T snv 2
rs4743763
ABCA1
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36 2
rs632153
APOA1 ; APOA1-AS
11 116839523 intron variant G/C;T snv 2
rs10488699
BUD13
11 116761784 intron variant C/T snv 1.0E-01 1
rs12363280
SIRT3
11 231980 intron variant C/A;G snv 1
rs1430583
UCP1
4 140565830 intron variant C/T snv 0.20 1