Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs6102059
LOC102724968
1.000 0.040 20 40600144 intergenic variant C/T snv 0.33 3
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 7
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62