Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11873890
TYMS
18 662135 intron variant A/G snv 8.2E-03 3.2E-02 4
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs8138057
PDXP
22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs34338511
NOTCH3
19 15184354 missense variant G/A;T snv 6.1E-04; 4.0E-06 3
rs34400162
GSTO2
10 104275312 missense variant G/A snv 5.6E-04 1.7E-03 3
rs760242
DHCR7
11 71435530 missense variant C/T snv 2.2E-04 6.3E-05 6
rs2243083
F2RL1
5 76833478 missense variant A/G;T snv 2.1E-04 2.6E-04 3
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs34183407
ALMS1
2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1000879
VIL1
2 218439407 intron variant G/A snv 4.1E-02 3
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
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
rs10808546 8 125483576 intron variant C/T snv 0.39 4