Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
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
rs2254819
ABCA1
9 104904133 intron variant T/C;G snv 3
rs2275544
ABCA1
9 104888931 intron variant T/C snv 0.14 3
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
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs4100654
ABCA1
9 104906960 intron variant T/C snv 8.3E-02 3
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
rs11789603
ABCA1
9 104884738 intron variant C/T snv 0.11 2
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs10115928
ABCA1
9 104888562 intron variant C/T snv 0.47 1
rs2575875
ABCA1
9 104900213 intron variant G/A snv 0.46 1
rs2777784
ABCA1
9 104898778 intron variant A/G snv 0.47 1