Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9957684 1.000 0.040 18 75154908 intergenic variant C/T snv 6.9E-02 2
rs10830956 1.000 0.040 11 92947847 intergenic variant C/T snv 0.33 1
rs12545984 1.000 0.040 8 19989748 intergenic variant C/T snv 0.16 1
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs1522813 1.000 0.040 2 226080466 regulatory region variant G/A snv 0.29 1
rs180088 1.000 0.040 17 69951455 intergenic variant T/A;C snv 0.71 1
rs180344 1.000 0.040 11 116742468 regulatory region variant T/C snv 0.34 1
rs1837842 1.000 0.040 8 20010779 intergenic variant T/C snv 0.23 1
rs376021 1.000 0.040 1 161555218 intron variant T/C snv 1.5E-04 1
rs4244457 1.000 0.040 8 20041535 intergenic variant C/G;T snv 1
rs4442164 1.000 0.040 8 20034670 regulatory region variant A/G snv 0.28 1
rs4449813 1.000 0.040 8 20045809 intergenic variant G/A snv 0.34 1
rs6995374 1.000 0.040 8 10468602 intergenic variant C/G snv 0.22 1
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 6
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 5
rs569805
ABCB11
1.000 0.040 2 168926370 intron variant A/T snv 0.73 2
rs916829
ABCC8
1.000 0.040 11 17418926 intron variant A/G;T snv 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs6720173
ABCG5 ; DYNC2LI1
0.827 0.080 2 43813262 missense variant G/C snv 0.21 0.21 5
rs4766587
ACACB
1.000 0.040 12 109247525 intron variant G/A snv 0.23 1
rs6606697
ACACB
1.000 0.040 12 109173915 intron variant A/G snv 0.48 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100