Disease: Coronary heart disease
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 8
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 12
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16