Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs2418736
NFATC3
16 68120959 intron variant G/A snv 0.28 4
rs247615 16 56950851 regulatory region variant A/G snv 0.23 3
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs4359427
NFATC3
16 68168844 intron variant C/G;T snv 3
rs4784744
CETP
16 56977273 non coding transcript exon variant G/A snv 0.30 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs7205804
CETP
16 56970977 intron variant G/A snv 0.34 4
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs11856159
ALDH1A2
15 58406811 intron variant C/A;G;T snv 4
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs261336
ALDH1A2 ; LIPC ; LIPC-AS1
15 58450219 intron variant G/A snv 0.81 5
rs261338
LIPC ; LIPC-AS1 ; ALDH1A2
15 58442806 intron variant A/G snv 0.83 5
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 5
rs415799
ALDH1A2
15 58398555 intron variant G/A snv 0.38 4