Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12917707 0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1317776692 14 104701619 missense variant C/G;T snv 4.4E-06 1
rs13293564 9 35166766 intron variant G/A;T snv 1
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs136161 0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs140511594 0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1427118369 2 227283830 missense variant G/A snv 4.0E-06 1.4E-05 1
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs1524107 0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02 6
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs17880135 21 31669690 upstream gene variant T/G snv 3.9E-02 1
rs17881180 21 31659974 non coding transcript exon variant C/T snv 3.8E-02 1
rs17883901 0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
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