| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1712572 | 1.000 | 0.080 | 3 | 106898231 | non coding transcript exon variant | A/C;G;T | snv | 1 | |||
| rs1393704451 | 1.000 | 0.080 | 2 | 109129746 | missense variant | A/G | snv | 1 | |||
| rs1015909000 | 1.000 | 0.080 | 9 | 14146790 | missense variant | A/G | snv | 1 | |||
| rs773029808 | 1.000 | 0.080 | 4 | 185626897 | missense variant | C/G | snv | 2.0E-05 | 1 | ||
| rs139155954 | 1.000 | 0.080 | 4 | 185662115 | missense variant | C/G;T | snv | 6.0E-05 | 1 | ||
| rs58973334 | 0.882 | 0.080 | 1 | 226883748 | missense variant | G/A | snv | 8.6E-03 | 1.4E-02 | 3 | |
| 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 | ||
| rs202178897 | 1.000 | 0.080 | 1 | 226885596 | missense variant | G/A;T | snv | 1.2E-04; 4.0E-06 | 1 | ||
| rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
| rs1215971988 | 1.000 | 0.080 | 1 | 226885618 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs778936527 | 0.925 | 0.080 | 1 | 226885669 | missense variant | G/A | snv | 2.4E-05 | 7.0E-06 | 2 | |
| rs28936379 | 0.807 | 0.120 | 1 | 226888977 | missense variant | A/C;G;T | snv | 4.0E-06 | 10 | ||
| rs63749884 | 0.851 | 0.160 | 1 | 226888979 | missense variant | G/A | snv | 5 | |||
| rs1482790603 | 1.000 | 0.080 | 1 | 226891284 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs1281129992 | 0.882 | 0.080 | 21 | 25891730 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs1223904774 | 0.790 | 0.120 | 21 | 25891772 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 8 | |
| rs63749964 | 0.851 | 0.080 | 21 | 25891783 | missense variant | A/C | snv | 4 | |||
| rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 17 | |||
| rs63750066 | 0.763 | 0.160 | 21 | 25891796 | missense variant | C/T | snv | 9.5E-05 | 6.3E-05 | 9 | |
| rs63751039 | 0.776 | 0.200 | 21 | 25891855 | missense variant | T/C | snv | 8 | |||
| rs63750064 | 0.925 | 0.080 | 21 | 25897605 | missense variant | C/G;T | snv | 2 | |||
| rs193922916 | 0.827 | 0.080 | 21 | 25897619 | missense variant | G/A;C | snv | 6 | |||
| rs63750847 | 0.790 | 0.120 | 21 | 25897620 | missense variant | C/T | snv | 4.5E-04 | 3.0E-04 | 8 | |
| rs572842823 | 0.763 | 0.160 | 21 | 25897626 | missense variant | T/A;G | snv | 11 |