Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 6
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs7205804
CETP
16 56970977 intron variant G/A snv 0.34 6
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 5
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 5
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 5
rs1558861 11 116736721 regulatory region variant C/G;T snv 5
rs1748197
DOCK7
1 62590441 intron variant G/A snv 0.42 5
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32 5
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs2280401
SNORD35B ; RPS11
19 49496752 intron variant G/A snv 0.12 5
rs2545801
GRK6
5 177414338 intron variant T/C snv 0.56 5
rs261334
LIPC ; ALDH1A2 ; LIPC-AS1
15 58434545 intron variant G/C snv 0.73 5
rs261336
ALDH1A2 ; LIPC ; LIPC-AS1
15 58450219 intron variant G/A snv 0.81 5
rs261338
LIPC ; LIPC-AS1 ; ALDH1A2
15 58442806 intron variant A/G snv 0.83 5
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73 5