Disease: Coronary Artery Disease
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 9
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 9
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 5
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 6
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs2281719
GALNT2
1.000 0.040 1 230161913 intron variant C/T snv 0.45 4
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs2880301
TPTE2
1.000 0.040 13 19526394 intron variant C/T snv 4
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 12
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 22
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 8
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 5
rs2908290
LOC105375257 ; GCK
1.000 0.040 7 44176538 intron variant G/A snv 0.43 3
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38