Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs12341993
ABCA1
9 104896629 intron variant C/A;T snv 3
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 3
rs13284054
ABCA1
9 104906792 intron variant T/C snv 0.12 3
rs13290420
ABCA1
9 104886684 intron variant T/C snv 0.16 3
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs2254819
ABCA1
9 104904133 intron variant T/C;G snv 3
rs2275544
ABCA1
9 104888931 intron variant T/C snv 0.14 3
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
rs2777795
ABCA1
9 104910084 intron variant G/A snv 8.8E-02 3
rs3847300
ABCA1
9 104886149 intron variant G/A snv 0.12 3
rs3847305
ABCA1
9 104894972 intron variant G/C snv 0.25 3
rs3858076
ABCA1
9 104893841 intron variant A/C snv 0.20 3
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs4100654
ABCA1
9 104906960 intron variant T/C snv 8.3E-02 3
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs4149269
ABCA1
9 104884840 intron variant A/G snv 0.41 3
rs4149272
ABCA1
9 104880006 intron variant C/G;T snv 0.48 3
rs4149273
ABCA1
9 104879930 intron variant T/C snv 0.45 3
rs35233375
ACADS
12 120739357 missense variant G/A snv 7.0E-06 3
rs16942333
ACAN
15 88845033 intron variant A/G snv 3.3E-02 3
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9