Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs188675529 | 0.827 | 0.240 | 16 | 67842794 | missense variant | C/G;T | snv | 1.6E-03 | 6.0E-04 | 11 | |
rs121918258 | 0.851 | 0.200 | 6 | 49457801 | missense variant | C/A;T | snv | 5 | |||
rs727504020 | 0.882 | 0.200 | 6 | 49451591 | stop gained | G/A;C | snv | 4.0E-05; 2.4E-05 | 4 | ||
rs748129702 | 1.000 | 0.080 | 6 | 49451555 | stop gained | C/A | snv | 8.0E-06 | 7.0E-06 | 2 |