Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs6726798
VIL1
2 218436132 intron variant A/C snv 0.94 3
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs691960
CYP27A1
2 218809281 intron variant G/T snv 7.0E-02 3
rs3729693
PIK3CA
3 179230408 intron variant A/G snv 1.0E-02 4.1E-02 3
rs4695266
CORIN
4 47670263 intron variant T/A;C snv 3
rs2243083
F2RL1
5 76833478 missense variant A/G;T snv 2.1E-04 2.6E-04 3
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs1936800 6 127114919 intron variant C/T snv 0.51 4
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs11974409
TBL2
0.925 0.120 7 73575060 intron variant A/G snv 0.16 6
rs13232120
TBL2
0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11 6
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 6
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs7811025 7 99788078 upstream gene variant C/T snv 4.8E-02 4
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 3
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11570892
LPL
8 19966106 3 prime UTR variant A/G;T snv 3