| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3025000 | 1.000 | 0.120 | 6 | 43778432 | non coding transcript exon variant | C/T | snv | 0.29 | 0.23 | 1 | |
| rs25648 | 0.742 | 0.320 | 6 | 43771240 | synonymous variant | C/G;T | snv | 8.5E-06; 0.16 | 11 | ||
| rs777846438 | 0.925 | 0.240 | 6 | 43780801 | splice region variant | C/T | snv | 4.4E-05 | 6.3E-05 | 2 | |
| 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 | ||
| rs140461341 | 6 | 43782078 | missense variant | G/A | snv | 3.6E-05 | 4.2E-05 | 2 | |||
| rs376388064 | 6 | 43782006 | missense variant | C/T | snv | 2.8E-05 | 3.5E-05 | 1 | |||
| rs141138308 | 1.000 | 0.040 | 6 | 43780784 | missense variant | C/A;T | snv | 4.0E-06; 2.8E-05 | 1 | ||
| rs541717889 | 6 | 43770888 | missense variant | G/C | snv | 2.1E-05 | 1 | ||||
| rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 | ||||
| rs1243046808 | 0.925 | 0.160 | 6 | 43770758 | missense variant | C/G;T | snv | 2.0E-05; 9.8E-06 | 2 | ||
| rs1201894677 | 6 | 43770833 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
| rs766474822 | 0.925 | 0.080 | 6 | 43770990 | missense variant | G/A | snv | 1.4E-05 | 2.1E-05 | 2 | |
| rs1365501228 | 1.000 | 0.080 | 6 | 43770732 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
| rs554561071 | 6 | 43777513 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 1 | |||
| rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
| rs748352475 | 0.925 | 0.160 | 6 | 43777546 | missense variant | C/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs138551969 | 1.000 | 0.040 | 6 | 43780749 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 4 | |
| rs1404013760 | 1.000 | 0.040 | 6 | 43771137 | missense variant | G/C | snv | 8.9E-06 | 1 | ||
| rs752907384 | 0.827 | 0.200 | 6 | 43782077 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
| rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
| rs1443465532 | 0.882 | 0.080 | 6 | 43774362 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs1287276985 | 0.790 | 0.200 | 6 | 43782020 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 7 | |
| rs374057152 | 0.925 | 0.200 | 6 | 43777592 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 |