Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4363657
SLCO1B1
12 21215788 intron variant T/C snv 0.18 5
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
rs1012657750
SELENBP1
1 151368294 missense variant G/C snv 2
rs11961407
CCHCR1
6 31154630 missense variant G/A snv 3.0E-03 1.3E-02 2
rs1249051329
SELENBP1
1 151369834 synonymous variant T/C snv 3.5E-05 2
rs1263163 11 116802796 intergenic variant G/A snv 0.10 2
rs1289389
SLC15A1
13 98684036 3 prime UTR variant C/T snv 0.18 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
rs5104
APOA4
11 116821618 missense variant C/T snv 0.80 0.85 2
rs632153
APOA1 ; APOA1-AS
11 116839523 intron variant G/C;T snv 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
rs10488699
BUD13
11 116761784 intron variant C/T snv 1.0E-01 1
rs1121923
LPL
8 19951924 synonymous variant G/A snv 3.3E-02 5.6E-02 1
rs11542035
APOE
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs12363280
SIRT3
11 231980 intron variant C/A;G snv 1
rs1430583
UCP1
4 140565830 intron variant C/T snv 0.20 1
rs1685354
UCP3
11 74002546 intron variant A/G snv 0.30 1
rs2075294
ZPR1
11 116787406 intron variant G/T snv 3.5E-02 1
rs217428
NPC1L1
7 44515974 intron variant T/G snv 0.21 0.26 1
rs217434
NPC1L1
7 44513639 synonymous variant A/G snv 0.16 0.17 1