Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906686 | 0.742 | 0.320 | 2 | 165310413 | missense variant | C/A;T | snv | 23 | |||
rs121909323 | 0.790 | 0.160 | 19 | 13277122 | stop gained | G/A | snv | 8 | |||
rs786200962 | 0.827 | 0.120 | 19 | 13298768 | frameshift variant | A/- | del | 7 | |||
rs786200963 | 0.827 | 0.200 | 19 | 13371683 | splice region variant | C/T | snv | 6 | |||
rs796053124 | 0.882 | 0.080 | 2 | 165354232 | missense variant | G/T | snv | 4 | |||
rs863224852 | 0.882 | 0.160 | 19 | 13359680 | missense variant | C/T | snv | 2 | |||
rs1805031 | 0.851 | 0.080 | 2 | 151880879 | missense variant | C/A | snv | 4.7E-04 | 7.3E-04 | 2 | |
rs121908226 | 0.925 | 0.120 | 19 | 13231847 | missense variant | C/T | snv | 1 | |||
rs137852620 | 0.925 | 0.080 | 5 | 36674080 | missense variant | T/A;G | snv | 1 |