Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397516354 | 0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 | 8 | ||
rs397516349 | 0.807 | 0.080 | 19 | 55154145 | missense variant | C/T | snv | 1.6E-05 | 6 | ||
rs727503504 | 0.807 | 0.080 | 19 | 55154071 | missense variant | G/A;C | snv | 6 | |||
rs267607129 | 0.925 | 0.040 | 19 | 55151912 | missense variant | G/C | snv | 2 | |||
rs267607130 | 0.925 | 0.040 | 19 | 55157052 | missense variant | T/G | snv | 2 | |||
rs777177571 | 1.000 | 0.040 | 19 | 55154766 | missense variant | G/C | snv | 1.6E-05 | 2.1E-05 | 1 |