Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587777308 | 0.763 | 0.040 | 5 | 161873196 | missense variant | G/A | snv | 14 | |||
rs118192211 | 0.790 | 0.080 | 20 | 63439644 | missense variant | G/A;C | snv | 9 | |||
rs121909674 | 0.790 | 0.080 | 5 | 162153132 | stop gained | C/T | snv | 8 | |||
rs587777057 | 0.827 | 0.040 | 16 | 56336744 | missense variant | G/A | snv | 8 | |||
rs886039903 | 0.807 | 0.200 | 3 | 192335434 | missense variant | C/T | snv | 6 | |||
rs1057518801 | 0.851 | 0.080 | 2 | 165130238 | missense variant | A/G | snv | 5 | |||
rs796053134 | 0.827 | 0.080 | 2 | 165374737 | missense variant | T/C | snv | 5 | |||
rs796052493 | 0.851 | 0.040 | 5 | 161895668 | missense variant | G/A;T | snv | 4 | |||
rs796053216 | 0.851 | 0.160 | 12 | 51790401 | stop gained | G/A;T | snv | 4 | |||
rs587777164 | 0.882 | 0.080 | 14 | 62950522 | missense variant | C/T | snv | 3 |