Disease: Serum HDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10501321
MADD-AS1 ; MADD
11 47273075 intron variant T/C snv 0.42 2
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 3
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs10773105
SCARB1
12 124799220 intron variant C/T snv 0.63 2
rs10773112
SCARB1
12 124853983 intron variant C/T snv 0.63 2
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs10818782
GABBR2
9 98325004 intron variant G/A snv 0.60 2
rs1084651 6 160668785 intron variant G/A snv 0.23 2
rs10846743
SCARB1
12 124825759 intron variant G/A snv 3.1E-02 2
rs10891841
CADM1
11 115361021 intron variant T/G snv 1.6E-02 2
rs10940493
IL6ST
5 55942083 intron variant C/A;G snv 2
rs10954843
NRG1
8 32419595 intron variant G/A snv 0.97 2
rs11065633
ATP2A2
12 110348445 3 prime UTR variant C/T snv 2.3E-02 2
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10 2
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs1109166
LCAT ; SLC12A4
16 67943479 5 prime UTR variant T/C snv 0.32 3
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs11216162
SIK3
11 116857561 non coding transcript exon variant G/A snv 0.17 3
rs11216230
SIK3
11 117014073 intron variant G/A snv 3.1E-02 2
rs11217785
POU2F3 ; LOC105369531
11 120281882 intron variant C/T snv 0.33 2
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs11236530
DGAT2
11 75778359 intron variant C/A snv 0.11 2