| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs772953044 | 0.925 | 0.120 | 1 | 6333503 | missense variant | T/C;G | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs1465262924 | 0.925 | 0.240 | 1 | 6281155 | missense variant | T/G | snv | 2 | |||
| rs1314714440 | 1.000 | 0.080 | 1 | 6349787 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 1 | |
| rs766402526 | 1.000 | 0.080 | 1 | 6339505 | missense variant | C/A;T | snv | 1.2E-05; 8.0E-06 | 1 | ||
| rs769564038 | 1.000 | 0.080 | 1 | 6339568 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs909221872 | 1 | 6349856 | missense variant | G/T | snv | 1 | |||||
| rs758821654 | 1.000 | 0.040 | 1 | 6339437 | synonymous variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs765693356 | 1.000 | 0.040 | 1 | 6339527 | synonymous variant | G/A | snv | 1.2E-05 | 1 | ||
| rs368731455 | 1.000 | 0.040 | 1 | 6281212 | missense variant | C/T | snv | 2.0E-05 | 1 | ||
| rs1034220998 | 1.000 | 0.040 | 1 | 6339497 | synonymous variant | G/A | snv | 1 | |||
| rs993269089 | 1.000 | 0.040 | 1 | 6385564 | missense variant | A/C;T | snv | 4.0E-06 | 1 |