Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs1199475313
ADRB3
0.851 0.040 8 37966277 missense variant T/C snv 7.0E-06 4
rs12040273
GALNT2
0.882 0.040 1 230063651 intron variant C/T snv 0.28 3
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs12050217
BDKRB1
0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1223493898
HNF4A
0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs12344245
FAM189A2
0.882 0.040 9 69340801 intron variant A/G snv 0.12 3
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs12704673
CALCR
0.882 0.040 7 93525009 intron variant A/G;T snv 0.27 3
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1310478538
C3
0.851 0.080 19 6713295 missense variant C/G snv 1.4E-05 4
rs13144478 0.882 0.040 4 115275150 regulatory region variant A/T snv 5.5E-02 4
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
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1351855165
DUOX2
0.882 0.040 15 45111550 synonymous variant G/A snv 3
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs138760780
CDK18
0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 3
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs1411364031
TNF
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06 3