Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11824953
MMP13
11 102949239 intron variant C/G snv 2.7E-02 3
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs2923084
CAND1.11 ; AMPD3
11 10367235 intron variant A/G snv 0.29 2
rs12274248
PDGFD
11 103954382 intron variant C/T snv 4.2E-02 2
rs34400162
GSTO2
10 104275312 missense variant G/A snv 5.6E-04 1.7E-03 3
rs4743758
NIPSNAP3A
9 104753533 intron variant C/T snv 0.37 1
rs2494748
AKT1
14 104792555 intron variant C/T snv 0.51 0.48 2
rs2740480
ABCA1
9 104800276 intron variant G/A snv 0.60 1
rs45490496 14 104806341 downstream gene variant A/T snv 0.45 2
rs4983559 14 104810872 downstream gene variant G/A;C snv 2
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs3824477
ABCA1
9 104826047 intron variant G/A snv 5.8E-02 1
rs3780543
ABCA1
9 104826291 intron variant A/G snv 0.23 2
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs7024300
ABCA1
9 104827286 intron variant C/T snv 5.8E-02 1
rs4149307
ABCA1
9 104827463 intron variant C/T snv 0.34 1
rs2853579
ABCA1
9 104828991 synonymous variant G/T snv 0.20 0.23 3
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 3
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2000069
ABCA1
9 104873588 intron variant C/G;T snv 2
rs4149273
ABCA1
9 104879930 intron variant T/C snv 0.45 3
rs4149272
ABCA1
9 104880006 intron variant C/G;T snv 0.48 3
rs11789603
ABCA1
9 104884738 intron variant C/T snv 0.11 3