Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs738791 0.851 0.120 22 23775338 intron variant C/T snv 0.37 6
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs377444977 0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 17
rs3212948 0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31