Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3783567 2 112788378 upstream gene variant G/A;T snv 3
rs3847300
ABCA1
9 104886149 intron variant G/A snv 0.12 3
rs3847305
ABCA1
9 104894972 intron variant G/C snv 0.25 3
rs3858076
ABCA1
9 104893841 intron variant A/C snv 0.20 3
rs4100654
ABCA1
9 104906960 intron variant T/C snv 8.3E-02 3
rs4149269
ABCA1
9 104884840 intron variant A/G snv 0.41 3
rs4149272
ABCA1
9 104880006 intron variant C/G;T snv 0.48 3
rs4149273
ABCA1
9 104879930 intron variant T/C snv 0.45 3
rs581080
TTC39B
9 15305380 intron variant G/C snv 0.72 3
rs7120078
APLNR
11 57239072 upstream gene variant A/G snv 1.5E-02 3
rs7241918
LOC105372112
18 49634583 intergenic variant G/A;T snv 3
rs7518440
ARNT
1 150818286 non coding transcript exon variant A/G;T snv 3
rs7941030 11 122651667 upstream gene variant T/C snv 0.39 3
rs874565
LIPG
18 49562320 synonymous variant C/A;T snv 9.4E-03 3
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv 3
rs9836225
MGLL
3 127797551 intron variant C/T snv 7.4E-03 3
rs9984764
APP
21 26125180 intron variant G/A snv 1.1E-02 3
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4
rs11571111
REN
1 204161105 intron variant C/A snv 5.0E-03 4
rs11635491
LIPC ; ALDH1A2
15 58427542 intron variant G/A snv 0.27 4
rs11873890
TYMS
18 662135 intron variant A/G snv 8.2E-03 3.2E-02 4
rs12285095
ZPR1
11 116787315 non coding transcript exon variant T/G snv 9.8E-02 4
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10 4
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 4