Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs255049
DPEP3
1.000 0.040 16 67979568 intron variant T/C snv 0.34 3
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87 3
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 3
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs9891572 1.000 0.040 17 2525214 intergenic variant C/T snv 0.17 3
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 3
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 3
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 4
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 6
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8