| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1444669684 | 0.658 | 0.480 | 9 | 21994285 | missense variant | C/A;T | snv | 36 | |||
| rs3731249 | 0.683 | 0.320 | 9 | 21970917 | missense variant | C/A;G;T | snv | 2.1E-02 | 22 | ||
| rs771138120 | 0.827 | 0.120 | 9 | 21971191 | missense variant | G/A;C;T | snv | 9.1E-06; 4.5E-06 | 13 | ||
| rs3088440 | 0.776 | 0.240 | 9 | 21968160 | 3 prime UTR variant | G/A | snv | 0.13 | 12 | ||
| rs3731239 | 0.763 | 0.240 | 9 | 21974219 | intron variant | A/G | snv | 0.26 | 9 | ||
| rs3731217 | 0.763 | 0.320 | 9 | 21984662 | intron variant | A/C;T | snv | 9 | |||
| rs104894094 | 0.763 | 0.200 | 9 | 21971058 | missense variant | C/A;G;T | snv | 8.5E-06; 4.3E-06 | 7 | ||
| rs1453633223 | 0.807 | 0.080 | 9 | 21974503 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
| rs200863613 | 0.925 | 0.080 | 9 | 21971061 | missense variant | C/A;T | snv | 8.5E-05 | 3.7E-04 | 6 | |
| rs11515 | 0.882 | 0.040 | 9 | 21968200 | 3 prime UTR variant | C/A;G | snv | 4.0E-06; 0.88 | 6 | ||
| rs1289280947 | 0.851 | 0.080 | 9 | 21974571 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs757066045 | 0.882 | 0.040 | 9 | 21974725 | missense variant | C/T | snv | 8.2E-06 | 4 | ||
| rs121913387 | 0.827 | 0.160 | 9 | 21971187 | stop gained | G/A;C | snv | 4.6E-06 | 4 | ||
| rs878853646 | 0.882 | 0.080 | 9 | 21971106 | missense variant | C/A;T | snv | 4.3E-06; 8.6E-06 | 3 | ||
| rs774904310 | 0.925 | 0.080 | 9 | 21971055 | frameshift variant | C/- | delins | 3 | |||
| rs104894104 | 0.790 | 0.160 | 9 | 21971019 | missense variant | G/A;T | snv | 3 | |||
| rs3731246 | 0.882 | 0.120 | 9 | 21971990 | intron variant | C/G | snv | 0.11 | 3 | ||
| rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 3 | ||
| rs786204195 | 0.851 | 0.200 | 9 | 21974686 | missense variant | G/A;T | snv | 3 | |||
| rs774829510 | 0.882 | 0.040 | 9 | 21971046 | missense variant | C/A;T | snv | 3 | |||
| rs2518720 | 0.925 | 0.080 | 9 | 21978980 | intron variant | C/T | snv | 0.43 | 2 | ||
| rs1057519883 | 0.742 | 0.280 | 9 | 21971120 | missense variant | C/G;T | snv | 2 | |||
| rs3731245 | 0.925 | 0.120 | 9 | 21972446 | intron variant | C/T | snv | 6.6E-03 | 2 | ||
| rs1390902532 | 1.000 | 0.040 | 9 | 21968766 | missense variant | T/C | snv | 7.4E-06 | 7.0E-06 | 2 | |
| rs3731201 | 1.000 | 0.080 | 9 | 21988897 | intron variant | C/T | snv | 0.86 | 2 |