| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs762735676 | 1.000 | 0.040 | 17 | 31221945 | frameshift variant | TTT/-;TTTT | delins | 6.6E-05 | 1 | ||
| rs1565527302 | 1.000 | 0.040 | 11 | 70485988 | frameshift variant | TG/- | del | 1 | |||
| rs1557874046 | 1.000 | 0.040 | 1 | 151408807 | missense variant | T/G | snv | 1 | |||
| rs10497655 | 1.000 | 0.040 | 2 | 184597314 | intron variant | T/C;G | snv | 1 | |||
| rs370498156 | 1.000 | 0.040 | 1 | 151404903 | missense variant | T/C;G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs749548928 | 1.000 | 0.040 | 1 | 151408815 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 4 | |
| rs121908445 | 0.925 | 0.040 | 7 | 148147542 | missense variant | T/C | snv | 3.3E-04 | 1.7E-04 | 1 | |
| rs1418634444 | 1.000 | 0.040 | 1 | 151408777 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1557863430 | 1.000 | 0.040 | 1 | 151405229 | missense variant | T/C | snv | 1 | |||
| rs1557863440 | 1.000 | 0.040 | 1 | 151405233 | missense variant | T/C | snv | 1 | |||
| rs1557910728 | 1.000 | 0.040 | 1 | 151428233 | missense variant | T/C | snv | 1 | |||
| rs16976358 | 0.827 | 0.080 | 18 | 42611606 | intron variant | T/C | snv | 1.0E-02 | 1 | ||
| rs375045125 | 1.000 | 0.040 | 1 | 151429672 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs3756963 | 0.882 | 0.200 | 6 | 11021921 | intron variant | T/C | snv | 0.24 | 1 | ||
| rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs561369202 | 1.000 | 0.040 | 1 | 151428152 | missense variant | T/C | snv | 6.4E-05 | 1.4E-05 | 1 | |
| rs574158925 | 1.000 | 0.040 | 1 | 151427829 | missense variant | T/C | snv | 5.6E-05 | 2.8E-05 | 1 | |
| rs749270162 | 1.000 | 0.040 | 1 | 151406620 | missense variant | T/C | snv | 2.4E-05 | 1 | ||
| rs760211123 | 1.000 | 0.040 | 1 | 151405662 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs769581210 | 1.000 | 0.040 | 1 | 151405376 | missense variant | T/C | snv | 7.2E-05 | 3.5E-05 | 1 | |
| rs4307059 | 0.882 | 0.080 | 5 | 25967594 | intron variant | T/A;C | snv | 2 | |||
| rs4130047 | 0.925 | 0.080 | 18 | 43098270 | intron variant | T/A;C | snv | 1 | |||
| rs1557863546 | 1.000 | 0.040 | 1 | 151405263 | missense variant | T/A | snv | 1 | |||
| rs1557911386 | 1.000 | 0.040 | 1 | 151428357 | missense variant | T/A | snv | 1 |