Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3783613
VCAM1
0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 6
rs1411224107
SERPINE1
0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 4
rs148158093
RPL36A-HNRNPH2 ; GLA
0.925 0.200 X 101403828 missense variant G/A snv 2.2E-04 4.0E-04 3
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs397514624
COL4A1
0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 3
rs200786329
COL4A1
0.925 13 110201467 missense variant G/A snv 5.2E-05 1.7E-04 3
rs752596535
LDLR
0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs544456198
LDLR
0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs1558139
CYP4F2
0.851 0.160 19 15886754 intron variant G/A snv 0.46 6
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
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
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800576
THBD
0.925 0.080 20 23049378 missense variant C/T snv 2.0E-03 2.5E-03 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs5049
AGT
1.000 0.040 1 230714337 intron variant C/T snv 0.16 3