| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
| rs28936379 | 0.807 | 0.120 | 1 | 226888977 | missense variant | A/C;G;T | snv | 4.0E-06 | 10 | ||
| rs140501902 | 0.807 | 0.160 | 1 | 226883774 | missense variant | C/T | snv | 3.6E-03 | 3.4E-03 | 6 | |
| rs28936380 | 0.827 | 0.080 | 1 | 226885546 | missense variant | C/G;T | snv | 1.2E-05 | 5 | ||
| rs63749884 | 0.851 | 0.160 | 1 | 226888979 | missense variant | G/A | snv | 5 | |||
| rs58973334 | 0.882 | 0.080 | 1 | 226883748 | missense variant | G/A | snv | 8.6E-03 | 1.4E-02 | 3 | |
| rs778936527 | 0.925 | 0.080 | 1 | 226885669 | missense variant | G/A | snv | 2.4E-05 | 7.0E-06 | 2 | |
| rs1215971988 | 1.000 | 0.080 | 1 | 226885618 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1482790603 | 1.000 | 0.080 | 1 | 226891284 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs202178897 | 1.000 | 0.080 | 1 | 226885596 | missense variant | G/A;T | snv | 1.2E-04; 4.0E-06 | 1 | ||
| rs1393704451 | 1.000 | 0.080 | 2 | 109129746 | missense variant | A/G | snv | 1 | |||
| rs1712572 | 1.000 | 0.080 | 3 | 106898231 | non coding transcript exon variant | A/C;G;T | snv | 1 | |||
| rs139155954 | 1.000 | 0.080 | 4 | 185662115 | missense variant | C/G;T | snv | 6.0E-05 | 1 | ||
| rs773029808 | 1.000 | 0.080 | 4 | 185626897 | missense variant | C/G | snv | 2.0E-05 | 1 | ||
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
| rs958576773 | 1.000 | 0.080 | 6 | 33662534 | missense variant | G/A | snv | 1 | |||
| rs1015909000 | 1.000 | 0.080 | 9 | 14146790 | missense variant | A/G | snv | 1 | |||
| rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
| rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 23 | |||
| rs63750306 | 0.701 | 0.320 | 14 | 73173663 | missense variant | A/C;G;T | snv | 17 | |||
| rs17125721 | 0.763 | 0.120 | 14 | 73206470 | missense variant | A/G | snv | 1.5E-02 | 1.5E-02 | 14 | |
| rs63750082 | 0.732 | 0.120 | 14 | 73192712 | missense variant | G/C;T | snv | 8.0E-06 | 13 | ||
| rs63750083 | 0.732 | 0.160 | 14 | 73219177 | missense variant | C/A;T | snv | 13 | |||
| rs63750526 | 0.776 | 0.160 | 14 | 73192832 | missense variant | C/A | snv | 10 |