Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs467323 | 12 | 49955982 | 3 prime UTR variant | C/G;T | snv | 2 | |||||
rs3741559 | 1.000 | 0.160 | 12 | 49951193 | splice region variant | G/A | snv | 0.20 | 0.17 | 3 | |
rs1049305 | 0.925 | 0.160 | 7 | 30924207 | 3 prime UTR variant | G/C | snv | 0.52 | 4 | ||
rs113090017 | 0.882 | 0.200 | 12 | 100532538 | stop gained | C/A;G;T | snv | 4.0E-06; 2.4E-05 | 4 | ||
rs1131692245 | 0.925 | 0.160 | 19 | 35844109 | missense variant | C/T | snv | 7 | |||
rs757075712 | 0.763 | 0.200 | 10 | 58390856 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 15 | |
rs2066845 | 0.611 | 0.600 | 16 | 50722629 | missense variant | G/C;T | snv | 1.1E-02; 2.2E-04 | 46 |