| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1305315912 | 1.000 | 0.080 | 6 | 43770736 | synonymous variant | C/T | snv | 2 | |||
| rs777846438 | 0.925 | 0.240 | 6 | 43780801 | splice region variant | C/T | snv | 4.4E-05 | 6.3E-05 | 2 | |
| rs1365501228 | 1.000 | 0.080 | 6 | 43770732 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
| rs735286 | 6 | 43776884 | non coding transcript exon variant | C/T | snv | 0.23 | 1 | ||||
| rs376388064 | 6 | 43782006 | missense variant | C/T | snv | 2.8E-05 | 3.5E-05 | 1 | |||
| rs3025000 | 1.000 | 0.120 | 6 | 43778432 | non coding transcript exon variant | C/T | snv | 0.29 | 0.23 | 1 | |
| rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
| rs833068 | 0.851 | 0.120 | 6 | 43774790 | non coding transcript exon variant | G/A | snv | 0.36 | 4 | ||
| rs3024997 | 0.882 | 0.120 | 6 | 43777370 | non coding transcript exon variant | G/A | snv | 0.31 | 3 | ||
| rs766474822 | 0.925 | 0.080 | 6 | 43770990 | missense variant | G/A | snv | 1.4E-05 | 2.1E-05 | 2 | |
| rs3025053 | 0.925 | 0.120 | 6 | 43785588 | 3 prime UTR variant | G/A | snv | 8.6E-02 | 2 | ||
| rs140461341 | 6 | 43782078 | missense variant | G/A | snv | 3.6E-05 | 4.2E-05 | 2 | |||
| rs1421145908 | 6 | 43777618 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
| rs1201894677 | 6 | 43770833 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
| rs752153816 | 0.882 | 0.120 | 6 | 43780848 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 | 3 | ||
| rs3025036 | 1.000 | 0.080 | 6 | 43783932 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs914956206 | 0.882 | 0.080 | 6 | 43770762 | missense variant | G/A;T | snv | 4 | |||
| rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 | ||||
| rs1443465532 | 0.882 | 0.080 | 6 | 43774362 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs3025030 | 0.882 | 0.200 | 6 | 43782850 | non coding transcript exon variant | G/C | snv | 0.13 | 3 | ||
| rs1404013760 | 1.000 | 0.040 | 6 | 43771137 | missense variant | G/C | snv | 8.9E-06 | 1 | ||
| rs541717889 | 6 | 43770888 | missense variant | G/C | snv | 2.1E-05 | 1 | ||||
| rs1212415280 | 6 | 43771130 | missense variant | G/T | snv | 2.1E-05 | 2 | ||||
| rs1287276985 | 0.790 | 0.200 | 6 | 43782020 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 7 | |
| rs1413711 | 0.882 | 0.200 | 6 | 43772941 | intron variant | T/A;C | snv | 3 |