Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 3
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs2271293
NUTF2
1.000 0.040 16 67868167 intron variant G/A snv 0.11 3
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 6
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 3
rs9891572 1.000 0.040 17 2525214 intergenic variant C/T snv 0.17 3
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 3
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7