Disease: Triglycerides measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs11569302
CD40
20 46118465 intron variant C/G;T snv 4
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs16940391
LIPC
15 58507449 intron variant C/A;G snv 3
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs1859287
SUGP1
19 19311378 intron variant T/A;C;G snv 4
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2255141
GPAM
10 112174128 intron variant A/G;T snv 5
rs2304128
GMIP
19 19635342 intron variant G/C;T snv 5
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs34499590
LEPR
1 65616108 missense variant C/G;T snv 2.5E-03 3
rs34630693
LRP1
12 57212472 missense variant C/A;T snv 1.2E-05; 2.0E-05 4
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 5
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18