Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 9
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6