Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 10
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
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 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
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
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6