Disease: Serum LDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038095
HMGCR
5 75341886 intron variant A/T snv 0.38 3
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 3
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs10306137
PTGS1
9 122376185 intron variant C/T snv 1.8E-02 3
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs10474434
HMGCR
5 75348856 intron variant G/T snv 0.20 3
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10490626
LOC107985940
2 118078265 intergenic variant G/A snv 5.2E-02 3
rs10500212
PBX4
19 19612406 intron variant C/T snv 0.10 4
rs10788994 1 55035303 upstream gene variant C/T snv 0.20 3
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10858082
CELSR2
1 109256099 intron variant G/A snv 0.48 3
rs10888898
PCSK9
1 55050835 intron variant A/G snv 0.59 3
rs10916704
PLA2G5
1 20074498 intron variant G/A;T snv 3
rs11136341
PLEC
8 143969375 intron variant A/G snv 0.40 3
rs11206514
PCSK9
1 55050331 intron variant C/A snv 0.52 3
rs11207997
DOCK7 ; ANGPTL3
1 62596235 intron variant C/T snv 0.39 5
rs11220462
ST3GAL4
11 126374057 intron variant G/A snv 0.12 3
rs11224571
PGR
11 101047942 intron variant C/A snv 1.2E-02 3
rs11465759
IL23R ; C1orf141
1 67166721 intron variant T/G snv 2.4E-02 4
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs11563251
UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A5 ; UGT1A1 ; UGT1A4 ; UGT1A10 ; UGT1A8
2 233770738 3 prime UTR variant C/T snv 0.19 5
rs11568373
ABCB11
2 168944893 synonymous variant T/C snv 5.8E-03 2.6E-02 3