Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730882109 | 0.882 | 0.080 | 19 | 11116900 | missense variant | C/G;T | snv | 4.0E-06; 1.1E-04 | 5 | ||
rs746118995 | 0.882 | 0.080 | 19 | 11120143 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 5 | |
rs754536745 | 0.882 | 0.080 | 19 | 11120144 | missense variant | G/A;T | snv | 2.0E-05 | 5 | ||
rs769737896 | 0.851 | 0.080 | 19 | 11110759 | stop gained | C/A;G;T | snv | 4.0E-06; 4.0E-06; 8.0E-06 | 5 | ||
rs771019366 | 0.882 | 0.080 | 19 | 11102742 | missense variant | A/C;G | snv | 5 | |||
rs793888517 | 0.882 | 0.080 | 19 | 11102788 | splice donor variant | T/A;C | snv | 5 | |||
rs875989909 | 0.882 | 0.080 | 19 | 11107486 | missense variant | C/G | snv | 5 | |||
rs875989929 | 0.882 | 0.080 | 19 | 11116888 | missense variant | G/A;T | snv | 5 | |||
rs879254459 | 0.882 | 0.080 | 19 | 11102771 | missense variant | G/A | snv | 5 | |||
rs879254535 | 0.925 | 0.080 | 19 | 11105369 | missense variant | T/A;C;G | snv | 5 | |||
rs879254667 | 0.882 | 0.080 | 19 | 11106631 | missense variant | A/C | snv | 5 | |||
rs879254770 | 0.882 | 0.080 | 19 | 11110765 | splice donor variant | CGAAGGTG/- | delins | 5 | |||
rs879254867 | 0.882 | 0.080 | 19 | 11113420 | stop gained | G/A;C;T | snv | 5 | |||
rs879254900 | 0.882 | 0.080 | 19 | 11113612 | missense variant | T/C | snv | 5 | |||
rs1057516127 | 0.925 | 0.080 | 19 | 11123200 | stop gained | G/T | snv | 7.0E-06 | 4 | ||
rs1057519669 | 0.925 | 0.080 | 19 | 11113347 | missense variant | A/G | snv | 4 | |||
rs1057519670 | 0.925 | 0.080 | 19 | 11113406 | missense variant | A/T | snv | 4 | |||
rs1057519673 | 0.925 | 0.080 | 19 | 11113705 | frameshift variant | C/- | del | 4 | |||
rs1057519677 | 0.925 | 0.080 | 19 | 11120099 | missense variant | T/G | snv | 4 | |||
rs121908024 | 0.925 | 0.080 | 19 | 11100252 | stop gained | C/T | snv | 8.0E-06 | 4 | ||
rs121908040 | 0.851 | 0.080 | 19 | 11106652 | missense variant | G/A;T | snv | 1.2E-05 | 4 | ||
rs121908042 | 0.925 | 0.080 | 19 | 11105232 | missense variant | G/A;C;T | snv | 4.0E-06 | 4 | ||
rs121908044 | 0.925 | 0.080 | 19 | 11105527 | synonymous variant | C/G;T | snv | 4 | |||
rs137853964 | 0.925 | 0.080 | 19 | 11129602 | missense variant | G/A;T | snv | 1.0E-03 | 4 | ||
rs139624145 | 0.925 | 0.080 | 19 | 11113620 | missense variant | G/A;C;T | snv | 4.0E-05 | 4 |