| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
| rs749491856 | 1.000 | 6 | 43782071 | missense variant | A/C | snv | 1 | ||||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs1570360 | 0.641 | 0.680 | 6 | 43770093 | upstream gene variant | A/G | snv | 0.76 | 38 | ||
| rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
| rs3025033 | 0.807 | 0.360 | 6 | 43783338 | non coding transcript exon variant | A/G | snv | 0.18 | 6 | ||
| rs1284410244 | 0.925 | 0.040 | 6 | 43778482 | missense variant | A/G | snv | 7.0E-06 | 4 | ||
| rs138551969 | 1.000 | 0.040 | 6 | 43780749 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 4 | |
| rs1346131223 | 1.000 | 6 | 43777657 | missense variant | A/G | snv | 7.4E-06 | 1 | |||
| rs554561071 | 6 | 43777513 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 1 | |||
| rs13207351 | 0.851 | 0.280 | 6 | 43770057 | upstream gene variant | A/G;T | snv | 4 | |||
| rs1479430148 | 1.000 | 0.120 | 6 | 43784861 | 3 prime UTR variant | A/T | snv | 1 | |||
| rs2146323 | 0.752 | 0.480 | 6 | 43777358 | non coding transcript exon variant | C/A | snv | 0.31 | 13 | ||
| rs141138308 | 1.000 | 0.040 | 6 | 43780784 | missense variant | C/A;T | snv | 4.0E-06; 2.8E-05 | 1 | ||
| rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
| rs748352475 | 0.925 | 0.160 | 6 | 43777546 | missense variant | C/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| 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 | ||
| rs1243046808 | 0.925 | 0.160 | 6 | 43770758 | missense variant | C/G;T | snv | 2.0E-05; 9.8E-06 | 2 | ||
| rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
| rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
| rs3024994 | 0.776 | 0.120 | 6 | 43775770 | non coding transcript exon variant | C/T | snv | 3.8E-02 | 8 | ||
| rs3025035 | 0.851 | 0.240 | 6 | 43783622 | non coding transcript exon variant | C/T | snv | 0.14 | 4 | ||
| rs3025020 | 0.882 | 0.240 | 6 | 43781373 | non coding transcript exon variant | C/T | snv | 0.24 | 3 |