Source: CURATED
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs367956522 | 0.851 | 0.240 | 13 | 51949798 | splice acceptor variant | T/C | snv | 2.4E-05 | 7.7E-05 | 7 | |
| rs201497300 | 0.925 | 0.160 | 13 | 51946337 | missense variant | C/T | snv | 4.6E-05 | 2.8E-05 | 2 | |
| rs1021025464 | 1.000 | 0.160 | 13 | 52012013 | splice region variant | T/C | snv | 9.1E-05 | 1 | ||
| rs1038582488 | 1.000 | 0.160 | 13 | 51946405 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1045194246 | 1.000 | 0.160 | 13 | 51944303 | non coding transcript exon variant | A/C;T | snv | 4.1E-06; 4.1E-06 | 1 | ||
| rs1052485948 | 1.000 | 0.160 | 13 | 51949764 | missense variant | A/C;G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs1057516305 | 1.000 | 0.160 | 13 | 51970663 | stop gained | C/A | snv | 1 | |||
| rs1057516380 | 1.000 | 0.160 | 13 | 51958509 | stop gained | G/T | snv | 1 | |||
| rs1057516425 | 1.000 | 0.160 | 13 | 51950006 | splice donor variant | C/T | snv | 1 | |||
| rs1057516479 | 1.000 | 0.160 | 13 | 51941108 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
| rs1057516516 | 1.000 | 0.160 | 13 | 51975117 | stop gained | T/A;C | snv | 4.0E-06 | 1 | ||
| rs1057516844 | 1.000 | 0.160 | 13 | 51958363 | missense variant | G/A | snv | 1 | |||
| rs1057517024 | 1.000 | 0.160 | 13 | 51965035 | splice acceptor variant | T/C | snv | 1 | |||
| rs1057517233 | 1.000 | 0.160 | 13 | 51937395 | splice acceptor variant | T/C | snv | 1 | |||
| rs1057517310 | 1.000 | 0.160 | 13 | 51949710 | missense variant | C/A | snv | 1 | |||
| rs1057517351 | 1.000 | 0.160 | 13 | 51975169 | splice acceptor variant | C/A | snv | 7.0E-06 | 1 | ||
| rs1057520235 | 1.000 | 0.160 | 13 | 51950277 | missense variant | A/G | snv | 1 | |||
| rs1064797072 | 1.000 | 0.160 | 13 | 51944116 | missense variant | C/A | snv | 1 | |||
| rs1085307057 | 1.000 | 0.160 | 13 | 51958517 | stop gained | G/A | snv | 1 | |||
| rs1131691741 | 1.000 | 0.160 | 13 | 51937305 | missense variant | T/G | snv | 7.0E-06 | 1 | ||
| rs1160679283 | 1.000 | 0.160 | 13 | 51935660 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
| rs1169959260 | 1.000 | 0.160 | 13 | 51949681 | missense variant | A/C | snv | 7.0E-06 | 1 | ||
| rs1173050016 | 1.000 | 0.160 | 13 | 51964924 | missense variant | A/C | snv | 1 | |||
| rs1206016866 | 1.000 | 0.160 | 13 | 51944131 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1212479289 | 1.000 | 0.160 | 13 | 51960191 | missense variant | G/C;T | snv | 1 |