Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10 4
rs12341993
ABCA1
9 104896629 intron variant C/A;T snv 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 3
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 4
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs13284054
ABCA1
9 104906792 intron variant T/C snv 0.12 3
rs13290420
ABCA1
9 104886684 intron variant T/C snv 0.16 3
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04 3
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
rs1532625
CETP
16 56971389 splice region variant C/T snv 0.40 0.34 4
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs1540037
LOC105372112
18 49656294 TF binding site variant A/G snv 0.83 3
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs16942333
ACAN
15 88845033 intron variant A/G snv 3.3E-02 3
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
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
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8