Disease: Low density lipoprotein cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 3
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs12113155
PRKAG2
7 151607887 intron variant A/C;G snv 3
rs13465
ILF3
19 10692116 3 prime UTR variant A/C;G snv 3
rs598962
ABCD3
1 94451093 intron variant A/C;G snv 3
rs655246 1 109289661 downstream gene variant A/C;G snv 3
rs7162932
TPM1
15 63060452 intron variant A/C;G snv 3
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs387976
NECTIN2
1.000 0.080 19 44875803 intron variant A/C;T snv 4
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 3
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10888898
PCSK9
1 55050835 intron variant A/G snv 0.59 3
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs11136341
PLEC
8 143969375 intron variant A/G snv 0.40 3
rs11577931 1 109278262 downstream gene variant A/G snv 5.5E-02 3
rs11668319
MEF2B ; BORCS8 ; BORCS8-MEF2B
19 19185066 intron variant A/G snv 0.15 3
rs12087003
ABCA4
1 94037627 intron variant A/G snv 6.3E-02 3
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02 3
rs12269156
PRKCQ
10 6470618 intron variant A/G snv 3.4E-02 3
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 3
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 3