Disease: Coronary heart disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 4
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12 2
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs216172
SMG6
0.925 0.040 17 2223210 intron variant G/C snv 0.35 2
rs840616
LOC105373786
0.925 0.040 2 187331742 intron variant T/C snv 0.56 2
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 4
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 2
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 2
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs6841581
EDNRA
0.882 0.080 4 147480038 upstream gene variant G/A;T snv 3
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 2
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 2
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 2
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10