Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 10
rs66492417
ABCC6
0.882 0.240 16 16178909 stop gained G/T snv 10
rs72657692
ABCC6
0.851 0.280 16 16169667 missense variant C/G;T snv 4.1E-06; 2.5E-05 10
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs63750410
ABCC6
0.882 0.240 16 16155007 missense variant C/G;T snv 6.0E-06; 1.2E-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
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 9
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs181985043
PER2
0.790 0.240 2 238262991 missense variant G/A;T snv 4.0E-06 8
rs192518038
CLOCK
0.790 0.240 4 55547195 non coding transcript exon variant C/A;G snv 8
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs775381348
PSMA6
0.807 0.160 14 35308023 missense variant G/T snv 8
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs1053874
DNASE1 ; TRAP1
0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 7
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs1312546120
F5
0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 7
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs9267551
CLIC1 ; DDAH2
0.807 0.160 6 31730180 5 prime UTR variant C/G;T snv 7
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7