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 |