Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11635252 0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
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
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs1431648262 8 26756585 3 prime UTR variant G/C snv 1.2E-05 2
rs150924946 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799904 1.000 0.080 5 96429259 missense variant C/A;T snv 4.0E-06; 2.1E-03 2
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800544 0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs1917760 7 143262206 intron variant G/A;T snv 1.8E-02 1
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2059806 0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs2119882 0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5