Disease: Coronary heart disease
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 22
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 8
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 4
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 7
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 8
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 9
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 13
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 11
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22