Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1761667 0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18