Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
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
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs2271293
NUTF2
1.000 0.040 16 67868167 intron variant G/A snv 0.11 3
rs2338104
KCTD10
1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 3
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3