Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 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
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 5
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 5
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T 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
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
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs11569302
CD40
20 46118465 intron variant C/G;T snv 4
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 4