| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1413711 | 0.882 | 0.200 | 6 | 43772941 | intron variant | T/A;C | snv | 3 | |||
| rs3024997 | 0.882 | 0.120 | 6 | 43777370 | non coding transcript exon variant | G/A | snv | 0.31 | 3 | ||
| rs3025020 | 0.882 | 0.240 | 6 | 43781373 | non coding transcript exon variant | C/T | snv | 0.24 | 3 | ||
| rs3025030 | 0.882 | 0.200 | 6 | 43782850 | non coding transcript exon variant | G/C | snv | 0.13 | 3 | ||
| rs3025040 | 0.882 | 0.120 | 6 | 43785314 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
| rs374057152 | 0.925 | 0.200 | 6 | 43777592 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
| 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 | ||
| rs1212415280 | 6 | 43771130 | missense variant | G/T | snv | 2.1E-05 | 2 | ||||
| rs1243046808 | 0.925 | 0.160 | 6 | 43770758 | missense variant | C/G;T | snv | 2.0E-05; 9.8E-06 | 2 | ||
| rs1305315912 | 1.000 | 0.080 | 6 | 43770736 | synonymous variant | C/T | snv | 2 | |||
| rs1365501228 | 1.000 | 0.080 | 6 | 43770732 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
| rs140461341 | 6 | 43782078 | missense variant | G/A | snv | 3.6E-05 | 4.2E-05 | 2 | |||
| rs3025053 | 0.925 | 0.120 | 6 | 43785588 | 3 prime UTR variant | G/A | snv | 8.6E-02 | 2 | ||
| rs748352475 | 0.925 | 0.160 | 6 | 43777546 | missense variant | C/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
| rs766474822 | 0.925 | 0.080 | 6 | 43770990 | missense variant | G/A | snv | 1.4E-05 | 2.1E-05 | 2 | |
| rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
| rs777846438 | 0.925 | 0.240 | 6 | 43780801 | splice region variant | C/T | snv | 4.4E-05 | 6.3E-05 | 2 | |
| rs1201894677 | 6 | 43770833 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
| rs1229919945 | 1.000 | 0.040 | 6 | 43782041 | missense variant | T/C | snv | 1 | |||
| rs1346131223 | 1.000 | 6 | 43777657 | missense variant | A/G | snv | 7.4E-06 | 1 | |||
| rs1404013760 | 1.000 | 0.040 | 6 | 43771137 | missense variant | G/C | snv | 8.9E-06 | 1 | ||
| rs141138308 | 1.000 | 0.040 | 6 | 43780784 | missense variant | C/A;T | snv | 4.0E-06; 2.8E-05 | 1 | ||
| rs1421145908 | 6 | 43777618 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
| rs1479430148 | 1.000 | 0.120 | 6 | 43784861 | 3 prime UTR variant | A/T | snv | 1 |