Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918312 | 0.776 | 0.160 | 10 | 119672373 | missense variant | C/A;T | snv | 11 | |||
rs730880031 | 0.807 | 0.160 | 22 | 23767438 | missense variant | C/A;T | snv | 1.8E-05; 4.4E-06 | 7 | ||
rs397515323 | 0.851 | 0.080 | X | 24503479 | missense variant | G/A | snv | 7 | |||
rs797045050 | 0.807 | 0.120 | 2 | 240797715 | missense variant | C/T | snv | 6 | |||
rs765672269 | 0.851 | 0.120 | 16 | 1792338 | stop gained | C/A | snv | 7.0E-06 | 5 | ||
rs119467003 | 0.882 | 0.080 | 14 | 89993420 | missense variant | A/G | snv | 2.1E-05 | 4 | ||
rs121918551 | 0.882 | 0.200 | 12 | 53308095 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
rs397515432 | 0.882 | 0.080 | 8 | 74364270 | missense variant | G/A | snv | 3 | |||
rs121913605 | 0.925 | 0.080 | 1 | 161307306 | missense variant | G/C | snv | 1.2E-05 | 2 | ||
rs771096255 | 1.000 | 0.040 | 6 | 43640312 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
rs1060501920 | 1.000 | 0.040 | 1 | 11992662 | missense variant | A/G | snv | 1 | |||
rs776404901 | 1.000 | 0.040 | 1 | 11996236 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs749165928 | 1.000 | 0.040 | 17 | 15230925 | missense variant | G/A;T | snv | 1.2E-05 | 1 |