Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1565679039 0.701 0.400 12 47983399 stop gained T/A snv 45
rs886039469 0.701 0.560 10 76891709 missense variant T/C snv 35
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1554121443 0.742 0.280 6 33438873 stop gained C/T snv 29
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs137854466 0.724 0.320 15 48411280 stop gained G/A;C snv 4.0E-05; 8.0E-06 23
rs1425998598 0.763 0.240 17 67918802 missense variant G/A;C snv 1.2E-05 19
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs5751876 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs727503054 0.732 0.200 15 48420752 missense variant A/G;T snv 1.6E-05 15
rs121918327 0.776 0.240 4 122742955 stop gained C/T snv 2.8E-05 1.4E-05 12
rs775769424 0.776 0.280 11 66530934 frameshift variant TG/- del 1.4E-05 11
rs4803455 0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs79204362 0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 10
rs1557551678 0.882 0.160 1 42738421 missense variant C/A snv 9
rs193922219 0.763 0.280 15 48446701 splice region variant C/A;T snv 9
rs1057524237 0.851 0.280 1 102915626 splice region variant C/T snv 7
rs2946834 0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs2075555 0.807 0.240 17 50196930 intron variant T/A;G snv 6
rs57865060 0.827 0.160 2 38074704 missense variant C/T snv 1.1E-02 5.7E-03 6
rs13095226 0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5
rs12423791 0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5