Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs2853579
ABCA1
9 104828991 synonymous variant G/T snv 0.20 0.23 3
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs11789603
ABCA1
9 104884738 intron variant C/T snv 0.11 2
rs3847302
ABCA1
9 104886314 intron variant A/G snv 0.12 2
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 1
rs2472509
ABCA1
9 104921949 intron variant T/G snv 0.29 1
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 1
rs2740480
ABCA1
9 104800276 intron variant G/A snv 0.60 1
rs2777795
ABCA1
9 104910084 intron variant G/A snv 8.8E-02 1
rs3824477
ABCA1
9 104826047 intron variant G/A snv 5.8E-02 1
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 1
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 1
rs4149307
ABCA1
9 104827463 intron variant C/T snv 0.34 1
rs7024300
ABCA1
9 104827286 intron variant C/T snv 5.8E-02 1