Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 15
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 3
rs611917
CELSR2
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs6831256
DOK7
4 3471412 intron variant A/G snv 0.49 4
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 5
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs170444
ABCG1
21 42230346 intron variant A/G;T snv 2
rs2954032 8 125481150 intron variant A/G;T snv 2
rs17031710
ABCG8 ; LOC102725159
2 43843754 intron variant A/T snv 2.1E-02 4
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs11571111
REN
1 204161105 intron variant C/A snv 5.0E-03 4
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 3
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11