Disease: Triglycerides measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 6
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs438811
APOC1
19 44913484 non coding transcript exon variant C/T snv 0.29 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 4
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 4
rs10864728
GALNT2
1 230169168 intron variant A/G snv 0.50 3
rs483082
APOC1
1.000 0.080 19 44912921 non coding transcript exon variant G/T snv 0.28 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3
rs7897379
REEP3
10 63541965 intron variant T/C snv 0.43 3
rs10508921
ASAH2
10 50250948 intron variant C/T snv 9.7E-02 2