Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs17243641
LOC105376326 ; TRAF2 ; MIR4479
9 136886986 intron variant G/T snv 2.6E-03 5
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs17513478
RIPK1
6 3101321 intron variant G/A snv 5.7E-03 5
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2231555
SOCS6
18 70324020 intron variant C/T snv 8.3E-03 3
rs2239051
CACNA1C
12 2343026 intron variant A/G snv 2.0E-03 4
rs2254819
ABCA1
9 104904133 intron variant T/C;G snv 3
rs2275544
ABCA1
9 104888931 intron variant T/C snv 0.14 3
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
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
rs261341
LIPC ; ALDH1A2 ; LIPC-AS1
15 58439368 intron variant A/G snv 0.54 4
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs2777795
ABCA1
9 104910084 intron variant G/A snv 8.8E-02 3