Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs387906592
STAMBPL1 ; ACTA2
0.752 0.280 10 88941309 missense variant C/T snv 14
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs12713559
APOB
0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs144467873
APOB
0.776 0.120 2 21006289 missense variant G/A snv 1.7E-04 6.3E-05 9
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs544456198
LDLR
0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs2228314
SREBF2
0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs3783613
VCAM1
0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 6
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs1126742
CYP4A11
0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 4
rs1411224107
SERPINE1
0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 4
rs1800576
THBD
0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 4
rs148158093
RPL36A-HNRNPH2 ; GLA
0.925 0.200 X 101403828 missense variant G/A snv 2.2E-04 4.0E-04 3
rs200786329
COL4A1
0.925 13 110201467 missense variant G/A snv 5.2E-05 1.7E-04 3
rs397514624
COL4A1
0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 3
rs563985037
TTC21A ; GORASP1
3 39107505 missense variant C/T snv 4.2E-05 1
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16