| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs183334241 | 0.925 | 0.080 | 18 | 75288186 | missense variant | G/A;C | snv | 1.6E-04 | 2 | ||
| rs377767394 | 0.925 | 0.080 | 10 | 43113603 | missense variant | A/C | snv | 2 | |||
| rs377767414 | 0.925 | 0.080 | 10 | 43118397 | missense variant | G/A | snv | 2 | |||
| rs377767426 | 1.000 | 0.080 | 10 | 43119694 | missense variant | C/G | snv | 1.8E-04 | 1.0E-04 | 2 | |
| rs78081605 | 0.925 | 0.080 | 18 | 75288051 | missense variant | G/C | snv | 8.0E-06 | 7.0E-06 | 2 | |
| rs864622088 | 0.925 | 0.080 | 9 | 95459774 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
| rs867966048 | 1.000 | 0.080 | 1 | 161340637 | missense variant | G/A;C | snv | 2 | |||
| rs104886028 | 1.000 | 0.080 | 12 | 25227308 | missense variant | C/T | snv | 1 | |||
| rs121913309 | 1.000 | 0.080 | 10 | 43120164 | inframe deletion | TGTTTATGAAGA/- | delins | 1 | |||
| rs121913312 | 1.000 | 0.080 | 10 | 43114494 | inframe deletion | GAGCTG/- | del | 1 | |||
| rs121913313 | 1.000 | 0.080 | 10 | 43113626 | inframe deletion | TTCCCTGAGGAGGAGAAGTGCTTCTGC/- | delins | 1 | |||
| rs145633958 | 1.000 | 0.080 | 10 | 43100551 | missense variant | C/A;T | snv | 2.7E-03; 4.0E-06 | 1 | ||
| rs3026785 | 1.000 | 0.080 | 10 | 43130238 | 3 prime UTR variant | T/C | snv | 4.3E-02 | 1 | ||
| rs33927012 | 1.000 | 0.080 | 1 | 17027802 | missense variant | A/G | snv | 1.2E-02 | 9.3E-03 | 1 | |
| rs747844360 | 1.000 | 0.080 | 10 | 43112853 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs750371239 | 1.000 | 0.080 | 11 | 108252912 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs769177037 | 1.000 | 0.080 | 1 | 161328467 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs770599902 | 1.000 | 0.080 | 1 | 161362382 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs773631693 | 1.000 | 0.080 | 10 | 43106436 | missense variant | C/A | snv | 4.0E-06 | 1 | ||
| rs777122776 | 1.000 | 0.080 | 10 | 43114515 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 1 | ||
| rs9282655 | 1.000 | 0.080 | 16 | 68823545 | missense variant | T/C | snv | 1 | |||
| rs77939446 | 0.724 | 0.120 | 10 | 43113622 | missense variant | G/A;C;T | snv | 4.0E-06 | 15 | ||
| rs11214077 | 0.752 | 0.120 | 11 | 112087953 | missense variant | A/G | snv | 6.6E-03 | 6.7E-03 | 12 | |
| rs1057519855 | 0.776 | 0.120 | 11 | 533873 | missense variant | CT/AC;TC | mnv | 11 | |||
| rs377767406 | 0.776 | 0.120 | 10 | 43114491 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 9 |