| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387907196 | 0.807 | 0.080 | 9 | 37784953 | missense variant | C/G | snv | 2.0E-05 | 12 | ||
| rs141138948 | 0.807 | 0.120 | 9 | 37783993 | missense variant | T/C;G | snv | 4.1E-04 | 9 | ||
| rs137853063 | 0.882 | 0.080 | 14 | 96876033 | stop gained | C/G;T | snv | 6.4E-05; 4.0E-06 | 4 | ||
| rs868010710 | 0.851 | 0.080 | 14 | 96833502 | missense variant | A/G | snv | 4 | |||
| rs374550999 | 0.925 | 0.080 | 9 | 37784807 | missense variant | C/A;G | snv | 1.5E-04 | 2 | ||
| rs1266703941 | 0.925 | 0.080 | 13 | 37002522 | missense variant | G/A;C | snv | 8.2E-06; 4.1E-06 | 2 | ||
| rs1064794609 | 1.000 | 0.080 | 16 | 89647238 | stop gained | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 1 | ||
| rs1566713184 | 1.000 | 0.080 | 14 | 96860643 | stop gained | C/T | snv | 1 | |||
| rs371295780 | 1.000 | 0.080 | 14 | 96847326 | missense variant | A/G | snv | 2.8E-05 | 2.8E-05 | 1 | |
| rs771364038 | 1.000 | 0.080 | 14 | 96855353 | missense variant | G/A;T | snv | 2.4E-05; 4.0E-06 | 1 | ||
| rs772263867 | 1.000 | 0.080 | 14 | 96846143 | stop gained | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs772731615 | 1.000 | 0.080 | 14 | 96860628 | missense variant | C/T | snv | 2.0E-04 | 1 | ||
| rs773138218 | 1.000 | 0.080 | 14 | 96846144 | missense variant | G/A;C | snv | 3.2E-05 | 1 | ||
| rs779282547 | 1.000 | 0.080 | 14 | 96856576 | frameshift variant | AAAC/- | delins | 8.0E-06 | 7.0E-06 | 1 | |
| rs780789145 | 1.000 | 0.080 | 14 | 96833477 | frameshift variant | T/- | del | 4.0E-06 | 7.0E-06 | 1 |