| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs41293511 | 0.763 | 0.320 | 13 | 32363369 | missense variant | G/A;C | snv | 7.0E-06 | 1 | ||
| rs80359014 | 0.763 | 0.320 | 13 | 32362596 | missense variant | A/G;T | snv | 1 | |||
| rs1243010179 | 1.000 | 0.160 | 16 | 67616807 | missense variant | C/T | snv | 1 | |||
| rs121913409 | 0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv | 1 | |||
| rs267607071 | 0.925 | 0.320 | 2 | 216475315 | missense variant | G/A | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs121912657 | 0.683 | 0.480 | 17 | 7673806 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs778634417 | 1.000 | 0.160 | 2 | 178633467 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs2234584 | 0.882 | 0.240 | 11 | 32428521 | missense variant | G/A;T | snv | 3.9E-04; 2.8E-05 | 1 |