Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs261342
LIPC-AS1 ; LIPC ; ALDH1A2
15 58438954 intron variant G/A;C;T snv 5
rs2777795
ABCA1
9 104910084 intron variant G/A snv 8.8E-02 3
rs2819325
NOS1AP
1 162313721 intron variant G/A;C snv 3
rs28927680
BUD13
11 116748357 3 prime UTR variant C/G;T snv 4
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs289718
CETP
16 56976020 intron variant C/T snv 0.64 3
rs289719
CETP
16 56976029 intron variant T/C snv 0.66 3
rs2954031 8 125479491 intron variant G/T snv 0.42 4
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs2975634
NOD1
7 30452077 missense variant C/A;T snv 4.0E-06; 6.3E-03 3
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 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
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs34183407
ALMS1
2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6
rs34660894
LRP1 ; STAT6
12 57129111 intron variant G/A snv 2.3E-03 1.0E-02 5
rs35233375
ACADS
12 120739357 missense variant G/A snv 7.0E-06 3
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs35738419
RXRA
9 134411944 intron variant C/T snv 7.3E-04 5
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs3783567 2 112788378 upstream gene variant G/A;T snv 3