Disease: Triglycerides measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 6
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 4
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 3
rs2908290
LOC105375257 ; GCK
1.000 0.040 7 44176538 intron variant G/A snv 0.43 3