ZNF337
zinc finger protein 337
Summary
This gene encodes a zinc finger domain containing protein. The function of this protein has yet to be determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs369445290 | 20:25,655,705 | C/T | — | uncertain significance |
| rs769931874 | 20:25,655,706 | G/A | — | uncertain significance |
| rs35755622 | 20:25,655,765 | C/A | — | uncertain significance |
| rs1043876055 | 20:25,655,861 | T/C | — | uncertain significance |
| rs2065665445 | 20:25,655,898 | A/G | — | uncertain significance |
| rs150351850 | 20:25,655,936 | T/C | — | uncertain significance |
| rs1261820842 | 20:25,655,945 | A/G | — | uncertain significance |
| rs2515370881 | 20:25,655,972 | G/A | — | uncertain significance |
| rs761016141 | 20:25,656,033 | T/C | — | uncertain significance |
| rs1569004361 | 20:25,656,138 | C/T | — | uncertain significance |
| rs1214038114 | 20:25,656,212 | G/A | — | uncertain significance |
| rs780926326 | 20:25,656,215 | C/T | — | uncertain significance |
| rs901730704 | 20:25,656,281 | T/G | — | uncertain significance |
| rs761389961 | 20:25,656,338 | G/A | — | uncertain significance |
| rs1216057961 | 20:25,656,356 | C/T | — | uncertain significance |
| rs146168838 | 20:25,656,393 | A/T | — | uncertain significance |
| rs1158234446 | 20:25,656,394 | G/T | — | uncertain significance |
| rs139483169 | 20:25,656,440 | C/T | — | uncertain significance |
| rs773238260 | 20:25,656,524 | C/T | — | uncertain significance |
| rs150890810 | 20:25,656,582 | C/T | — | uncertain significance |
| rs139346597 | 20:25,656,599 | A/T | — | uncertain significance |
| rs557218253 | 20:25,656,688 | G/T | — | uncertain significance |
| rs746765447 | 20:25,656,758 | C/A | — | uncertain significance |
| rs575478110 | 20:25,656,794 | G/A | — | uncertain significance |
| rs201475832 | 20:25,656,807 | C/T | — | uncertain significance |
| rs200552425 | 20:25,656,860 | C/T | — | uncertain significance |
| rs760151388 | 20:25,656,905 | C/T | — | uncertain significance |
| rs763074566 | 20:25,656,910 | G/T | — | uncertain significance |
| rs2515378389 | 20:25,656,936 | T/C | — | uncertain significance |
| rs148965153 | 20:25,656,954 | C/G | — | uncertain significance |
| rs367982268 | 20:25,656,969 | G/C | — | uncertain significance |
| rs1600431536 | 20:25,657,002 | T/C | — | uncertain significance |
| rs747657294 | 20:25,657,028 | C/T | — | uncertain significance |
| rs769983601 | 20:25,657,062 | C/G | — | uncertain significance |
| rs140839485 | 20:25,657,106 | T/C | — | uncertain significance |
| rs200386201 | 20:25,657,232 | G/C | — | uncertain significance |
| rs200763441 | 20:25,657,280 | T/C | — | uncertain significance |
| rs372703486 | 20:25,657,302 | A/C | — | uncertain significance |
| rs2515381560 | 20:25,657,332 | G/A | — | uncertain significance |
| rs139565721 | 20:25,657,352 | C/T | — | likely benign |
| rs140373318 | 20:25,657,370 | C/T | — | uncertain significance |
| rs1479138490 | 20:25,657,422 | C/G | — | uncertain significance |
| rs2515382602 | 20:25,657,436 | G/C | — | uncertain significance |
| rs752042447 | 20:25,657,479 | C/T | — | uncertain significance |
| rs945455324 | 20:25,657,647 | G/C | — | uncertain significance |
| rs182272160 | 20:25,657,649 | C/T | — | uncertain significance |
| rs202151029 | 20:25,666,212 | G/C | — | uncertain significance |
| rs2065821622 | 20:25,666,214 | C/T | — | uncertain significance |
| rs2515413975 | 20:25,667,034 | C/T | — | uncertain significance |
| rs6138639 | 20:25,669,052 | C/T | — | — |
| rs74853405 | 20:25,675,318 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.