Disease: Triglycerides measurement
Source: ALL
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
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10518982
LIPC
15 58507555 intron variant A/G snv 2.2E-02 3
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs1713222 2 21048451 upstream gene variant A/G snv 0.82 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
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 9
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs28917504
CD4
12 6814956 missense variant A/G snv 1.5E-03 6.4E-03 4
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
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
rs4385188
CERT1
5 75438537 intron variant A/G snv 0.33 4
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs5020
SLC4A1
17 44255219 splice region variant A/G snv 3.2E-03 1.3E-02 3
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21