| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs374057152 | 0.925 | 0.200 | 6 | 43777592 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs1346131223 | 1.000 | 6 | 43777657 | missense variant | A/G | snv | 7.4E-06 | 1 | |||
| rs1421145908 | 6 | 43777618 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
| rs1188254133 | 0.851 | 0.240 | 6 | 43781990 | missense variant | T/G | snv | 7.0E-06 | 4 | ||
| rs748352475 | 0.925 | 0.160 | 6 | 43777546 | missense variant | C/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs1287276985 | 0.790 | 0.200 | 6 | 43782020 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 7 | |
| rs1284410244 | 0.925 | 0.040 | 6 | 43778482 | missense variant | A/G | snv | 7.0E-06 | 4 | ||
| rs1443465532 | 0.882 | 0.080 | 6 | 43774362 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
| rs833061 | 0.605 | 0.600 | 6 | 43769749 | upstream gene variant | C/G;T | snv | 42 | |||
| rs25648 | 0.742 | 0.320 | 6 | 43771240 | synonymous variant | C/G;T | snv | 8.5E-06; 0.16 | 11 | ||
| rs752907384 | 0.827 | 0.200 | 6 | 43782077 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
| rs833069 | 0.851 | 0.200 | 6 | 43774842 | non coding transcript exon variant | T/C;G | snv | 5 | |||
| rs914956206 | 0.882 | 0.080 | 6 | 43770762 | missense variant | G/A;T | snv | 4 | |||
| rs13207351 | 0.851 | 0.280 | 6 | 43770057 | upstream gene variant | A/G;T | snv | 4 | |||
| 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 | ||
| rs1413711 | 0.882 | 0.200 | 6 | 43772941 | intron variant | T/A;C | snv | 3 | |||
| rs1305315912 | 1.000 | 0.080 | 6 | 43770736 | synonymous variant | C/T | snv | 2 | |||
| rs1243046808 | 0.925 | 0.160 | 6 | 43770758 | missense variant | C/G;T | snv | 2.0E-05; 9.8E-06 | 2 | ||
| rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
| rs1365501228 | 1.000 | 0.080 | 6 | 43770732 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
| rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
| rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 | ||||
| rs1404013760 | 1.000 | 0.040 | 6 | 43771137 | missense variant | G/C | snv | 8.9E-06 | 1 |