Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 8
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11