Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 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
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 5
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 5
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 5
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs473224
LIPC-AS1 ; ALDH1A2 ; LIPC
15 58445142 intron variant T/A;G snv 5
rs485538
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448978 intron variant C/G;T snv 5
rs485671
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448935 intron variant A/C;T snv 5
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 5
rs588136
ALDH1A2 ; LIPC ; LIPC-AS1
15 58438299 intron variant C/G;T snv 5
rs7666097
KDR
4 55124971 intron variant T/A;C snv 5
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4