Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 5
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 3
rs255
LPL
8 19954390 intron variant T/C snv 0.17 0.18 3
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs4922115
LPL
8 19965319 3 prime UTR variant G/A snv 0.15 0.14 3
rs316
LPL
8 19960925 missense variant C/A;T snv 0.13; 4.0E-06 3
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs343
LPL
1.000 0.080 8 19953276 intron variant C/A snv 9.8E-02 8.1E-02 3
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10 4
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 4
rs3729693
PIK3CA
3 179230408 intron variant A/G snv 1.0E-02 4.1E-02 3