Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs2271293
NUTF2
1.000 0.040 16 67868167 intron variant G/A snv 0.11 3
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs255049
DPEP3
1.000 0.040 16 67979568 intron variant T/C snv 0.34 3
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 3
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87 3
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 4
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 3
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7