Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1234442507
TUBB1
1.000 0.040 20 59022915 frameshift variant AG/- del 4.0E-06 3
rs463312
TUBB1
1.000 0.040 20 59022915 missense variant A/C snv 7.7E-02 5.7E-02 4
rs7692387
GUCY1A1
0.925 0.080 4 155714157 intron variant G/A snv 0.16 5
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2138533
COL3A1 ; LOC105373791
1.000 0.120 2 188972486 upstream gene variant T/A;C snv 3
rs2359612
VKORC1
0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs5070
APOA1 ; APOA1-AS
0.882 0.160 11 116837304 intron variant A/G snv 0.56 0.60 5
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2266780
FMO3
0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22