| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2181874 | 1.000 | 0.080 | 20 | 54167939 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs868063722 | 1.000 | 0.080 | 10 | 94775077 | missense variant | C/T | snv | 1 | |||
| rs777175289 | 1.000 | 0.080 | 7 | 99664085 | synonymous variant | T/C | snv | 4.5E-06 | 1 | ||
| rs554326805 | 1.000 | 0.080 | 19 | 15647052 | missense variant | C/G;T | snv | 4.0E-06; 4.4E-05 | 1 | ||
| rs749777680 | 1.000 | 0.080 | 19 | 15645858 | missense variant | C/T | snv | 8.2E-06 | 1 | ||
| rs780092348 | 1.000 | 0.080 | 19 | 15644046 | missense variant | C/T | snv | 4.7E-06 | 1 | ||
| rs1077424 | 1.000 | 0.080 | 1 | 57344632 | intron variant | G/C | snv | 0.52 | 1 | ||
| rs11207010 | 1.000 | 0.080 | 1 | 57337214 | intron variant | G/C | snv | 0.41 | 1 | ||
| rs12061812 | 1.000 | 0.080 | 1 | 57336931 | intron variant | C/A | snv | 0.30 | 1 | ||
| rs12087888 | 1.000 | 0.080 | 1 | 57337087 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs17425189 | 1.000 | 0.080 | 1 | 57397277 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs267650 | 1.000 | 0.080 | 1 | 57330108 | intron variant | T/C | snv | 0.36 | 1 | ||
| rs3909556 | 1.000 | 0.080 | 1 | 57381313 | intron variant | C/A;T | snv | 1 | |||
| rs776310470 | 1.000 | 0.080 | 5 | 10680713 | synonymous variant | G/A | snv | 4.6E-04 | 5.8E-04 | 1 | |
| rs5879422 | 1.000 | 0.080 | 6 | 117463495 | intron variant | -/GT | delins | 0.54 | 1 | ||
| rs1732786 | 1.000 | 0.080 | 12 | 113057841 | 5 prime UTR variant | G/A | snv | 0.65 | 1 | ||
| rs778040733 | 1.000 | 0.080 | 4 | 109988662 | missense variant | T/C | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs121913420 | 1.000 | 0.080 | 7 | 55174737 | missense variant | G/A | snv | 1 | |||
| rs121913427 | 1.000 | 0.080 | 7 | 55174773 | missense variant | G/A;C | snv | 1 | |||
| rs121913464 | 1.000 | 0.080 | 7 | 55174792 | missense variant | C/A | snv | 1 | |||
| rs121913466 | 1.000 | 0.080 | 7 | 55174762 | missense variant | T/C | snv | 1 | |||
| rs121913467 | 1.000 | 0.080 | 7 | 55174730 | stop gained | G/A | snv | 1 | |||
| rs1427028322 | 1.000 | 0.080 | 7 | 55163740 | missense variant | A/G | snv | 1 | |||
| rs376822837 | 1.000 | 0.080 | 7 | 55198761 | missense variant | G/A | snv | 3.6E-05 | 6.3E-05 | 1 | |
| rs397517086 | 1.000 | 0.080 | 7 | 55173986 | inframe deletion | AAC/- | del | 1 |