Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1206846668
FOLH1
0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs1208
NAT2
0.807 0.080 8 18400806 missense variant G/A;T snv 0.62; 4.0E-06 8
rs12115090
CRISPLD1
0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs121912777
CES1
0.851 0.080 16 55823661 missense variant C/A;G;T snv 4.8E-05; 1.2E-05; 8.0E-06 5
rs12232780
SMARCA4
0.807 0.080 19 11021404 non coding transcript exon variant G/A snv 0.23 6
rs1223493898
HNF4A
0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
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
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
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
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
rs12794714
CYP2R1
0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8