Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
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
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