Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12344245
FAM189A2
0.882 0.040 9 69340801 intron variant A/G snv 0.12 3
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs12526453
PHACTR1
0.827 0.160 6 12927312 intron variant C/G snv 0.27 5
rs12704673
CALCR
0.882 0.040 7 93525009 intron variant A/G;T snv 0.27 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs13306221
BDNF
0.851 0.120 11 27701142 intron variant C/T snv 5.9E-02 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs138760780
CDK18
0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 3
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 4
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs1541861
NOS3
0.925 0.040 7 151000245 intron variant C/A snv 0.70 2
rs16941382
GOSR2 ; LRRC37A2
0.882 0.040 17 46966142 intron variant T/C snv 0.15 3
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12 2
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8