Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1790349
DHCR7
0.882 0.040 11 71431304 intron variant T/C snv 0.19 4
rs763802417
NOX1
0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs1408888
DACH1
0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1866389
THBS4
0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs3732581
PARL
0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs544456198
LDLR
0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs6850
LOC105375259 ; PPIA
0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15