Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 7
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6