Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs2228146 0.925 0.120 1 154454574 missense variant G/A snv 1.3E-02; 4.0E-06 5.4E-02 3
rs5030718 0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs758130759 0.925 0.120 17 37699149 missense variant C/T snv 1.6E-05 1.4E-05 3
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1143770 0.882 0.200 11 122146890 intron variant C/T snv 0.53 4
rs11771443 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs11915160 0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 5
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1532624 0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7