| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2227589 | 0.925 | 0.120 | 1 | 173917078 | intron variant | C/T | snv | 9.6E-02 | 3 | ||
| rs542881762 | 1.000 | 0.080 | 1 | 173907528 | intron variant | C/G;T | snv | 2.8E-05 | 1 | ||
| rs398124401 | 0.695 | 0.480 | 4 | 55346393 | stop gained | G/A | snv | 1.2E-04 | 2.8E-05 | 26 | |
| rs121909562 | 1.000 | 0.080 | 1 | 173911942 | stop gained | G/A | snv | 1 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
| rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
| rs368927897 | 0.790 | 0.240 | 9 | 5072541 | missense variant | G/A;T | snv | 2.8E-05; 6.4E-05 | 9 | ||
| rs121909552 | 0.925 | 0.080 | 1 | 173914725 | missense variant | C/T | snv | 9.5E-05 | 1.7E-04 | 2 | |
| rs121909567 | 0.925 | 0.120 | 1 | 173914570 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 2 | |
| rs1248438558 | 0.925 | 0.120 | 13 | 113149020 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs1487411568 | 0.925 | 0.120 | 1 | 173903969 | missense variant | G/A;T | snv | 7.0E-06 | 2 | ||
| rs1170430756 | 1.000 | 0.080 | 1 | 173911987 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs1188571702 | 1.000 | 0.080 | 1 | 173903962 | missense variant | A/G | snv | 1 | |||
| rs121909546 | 1.000 | 0.080 | 1 | 173903978 | missense variant | C/T | snv | 1 | |||
| rs121909547 | 1.000 | 0.080 | 1 | 173914726 | missense variant | G/A;T | snv | 4.8E-05 | 1 | ||
| rs121909548 | 1.000 | 0.080 | 1 | 173904038 | missense variant | C/A;G | snv | 8.9E-04 | 1 | ||
| rs121909549 | 1.000 | 0.080 | 1 | 173904010 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs121909550 | 1.000 | 0.080 | 1 | 173904007 | missense variant | G/A;C | snv | 1 | |||
| rs121909551 | 1.000 | 0.080 | 1 | 173914743 | missense variant | G/A | snv | 8.2E-04 | 9.0E-04 | 1 | |
| rs121909554 | 1.000 | 0.080 | 1 | 173904011 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs121909555 | 1.000 | 0.080 | 1 | 173903968 | missense variant | G/A | snv | 1 | |||
| rs121909557 | 1.000 | 0.080 | 1 | 173904044 | missense variant | C/T | snv | 1 |