Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs13038305
CST3
0.925 0.080 20 23629625 intron variant C/T snv 0.21 5
rs36071027
EBF1
0.925 0.080 5 159017266 intron variant C/T snv 0.29 4
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs74830677
SCARB1
0.882 0.080 12 124800125 missense variant G/A snv 9.9E-04 6.7E-04 6
rs7896005
SIRT1
0.925 0.080 10 67891367 intron variant A/G;T snv 0.52; 8.0E-06 0.47 4
rs8192675
SLC2A2
0.925 0.080 3 171007094 intron variant T/C snv 0.42 5
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs3732581
PARL
0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs6850
LOC105375259 ; PPIA
0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
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