Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs34515106
PLEK
2 68380846 missense variant A/C snv 6.7E-03 1.9E-03 2
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 3
rs485671
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448935 intron variant A/C;T snv 5
rs11873890
TYMS
18 662135 intron variant A/G snv 8.2E-03 3.2E-02 4
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs12721054
APOC1
19 44919330 3 prime UTR variant A/G snv 3.7E-02 2
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2239051
CACNA1C
12 2343026 intron variant A/G snv 2.0E-03 4
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 3
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs261338
LIPC ; LIPC-AS1 ; ALDH1A2
15 58442806 intron variant A/G snv 0.83 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs28917504
CD4
12 6814956 missense variant A/G snv 1.5E-03 6.4E-03 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6