Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs16999051
PCSK2
0.882 0.280 20 17380837 intron variant C/T snv 0.13 3
rs6060566
NFS1 ; ROMO1
0.925 0.160 20 35700304 intron variant T/C snv 0.19 2
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs2115386
INSR
0.925 0.160 19 7196554 intron variant C/T snv 0.48 2
rs2000813
LIPG
0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 9
rs770572030
LIPG
0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5
rs599019 0.925 0.160 18 294495 intergenic variant C/A snv 0.78 2
rs11662496 1.000 0.120 18 43695432 intergenic variant A/G;T snv 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs1136287
SERPINF1
0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv 5
rs9896052 0.882 0.160 17 75422781 intergenic variant A/C snv 0.50 3
rs9913583
SERPINF1
0.925 0.120 17 1762036 5 prime UTR variant C/A snv 6.6E-02 2
rs12150053
SERPINF1
1.000 0.120 17 1761175 upstream gene variant T/A;C snv 1
rs12948385
SERPINF1
1.000 0.120 17 1761607 upstream gene variant G/A snv 0.26 1
rs1373054855
PECAM1
1.000 0.120 17 64370017 missense variant A/G snv 1.4E-05 1
rs17684886
ZNRF1
0.925 0.160 16 75052977 intron variant A/T snv 0.12 2