ZMYM6
zinc finger MYM-type containing 6
Summary
Predicted to enable DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200114922 | 1:35,452,702 | T/C | — | benign |
| rs1203210105 | 1:35,452,769 | G/A | — | uncertain significance |
| rs191963770 | 1:35,452,838 | T/C | — | uncertain significance |
| rs1200899408 | 1:35,452,869 | T/C | — | uncertain significance |
| rs16837147 | 1:35,452,986 | C/T | — | benign |
| rs772893416 | 1:35,453,057 | C/T | — | uncertain significance |
| rs1201032130 | 1:35,453,091 | A/C | — | uncertain significance |
| rs924818039 | 1:35,453,190 | T/C | — | uncertain significance |
| rs370031261 | 1:35,453,285 | G/A | — | uncertain significance |
| rs369530067 | 1:35,453,365 | A/G | — | likely benign |
| rs1237293902 | 1:35,453,396 | T/C | — | uncertain significance |
| rs536800175 | 1:35,453,618 | A/G | — | likely benign |
| rs61744853 | 1:35,453,651 | A/C | — | benign |
| rs541106336 | 1:35,453,671 | T/C | — | likely benign |
| rs61743186 | 1:35,453,771 | T/G | — | likely benign |
| rs141138840 | 1:35,453,877 | G/A | — | benign |
| rs144581211 | 1:35,453,878 | A/G | — | benign |
| rs61745582 | 1:35,454,115 | A/G | — | benign |
| rs370942660 | 1:35,454,246 | A/G | — | uncertain significance |
| rs1021275304 | 1:35,454,318 | A/G | — | likely benign |
| rs375427669 | 1:35,454,371 | C/T | — | uncertain significance |
| rs61741445 | 1:35,454,473 | C/G | — | benign |
| rs2523131064 | 1:35,454,507 | C/T | — | uncertain significance |
| rs2523140366 | 1:35,457,841 | G/C | — | uncertain significance |
| rs142539781 | 1:35,457,928 | G/A | — | uncertain significance |
| rs372430082 | 1:35,457,958 | G/C | — | uncertain significance |
| rs147786113 | 1:35,467,083 | C/T | intron variant | — |
| rs10158256 | 1:35,469,582 | T/C | — | likely benign |
| rs370957462 | 1:35,470,792 | A/G | — | uncertain significance |
| rs145546610 | 1:35,470,798 | C/T | — | likely benign |
| rs1475061234 | 1:35,470,809 | T/G | — | likely benign |
| rs10158284 | 1:35,470,877 | A/T | — | benign |
| rs774159523 | 1:35,472,571 | G/T | — | uncertain significance |
| rs1640993776 | 1:35,472,657 | C/G | — | uncertain significance |
| rs748842813 | 1:35,474,380 | C/T | — | uncertain significance |
| rs373960300 | 1:35,474,489 | C/T | — | uncertain significance |
| rs201963462 | 1:35,474,493 | C/G | — | uncertain significance |
| rs41266439 | 1:35,476,349 | C/T | — | benign |
| rs142879653 | 1:35,476,384 | G/C | — | uncertain significance |
| rs367908302 | 1:35,476,414 | T/C | — | uncertain significance |
| rs748001989 | 1:35,476,424 | C/T | — | uncertain significance |
| rs759091664 | 1:35,476,492 | C/A | — | uncertain significance |
| rs767315303 | 1:35,476,493 | C/A | — | uncertain significance |
| rs752388925 | 1:35,476,495 | C/T | — | uncertain significance |
| rs756028380 | 1:35,476,496 | G/A | — | uncertain significance |
| rs147439192 | 1:35,476,609 | T/G | — | benign |
| rs2521156203 | 1:35,477,504 | A/G | — | uncertain significance |
| rs35847987 | 1:35,477,551 | T/C | — | benign |
| rs768988738 | 1:35,478,075 | A/C | — | uncertain significance |
| rs1374742551 | 1:35,478,130 | G/C | — | uncertain significance |
| rs574713128 | 1:35,478,139 | C/G | — | uncertain significance |
| rs555176875 | 1:35,478,154 | A/G | — | uncertain significance |
| rs143135186 | 1:35,480,426 | T/C | — | uncertain significance |
| rs2521182739 | 1:35,480,447 | A/G | — | uncertain significance |
| rs2521182747 | 1:35,480,450 | G/T | — | uncertain significance |
| rs140404514 | 1:35,480,455 | T/C | — | uncertain significance |
| rs138190908 | 1:35,480,456 | G/A | — | uncertain significance |
| rs567405582 | 1:35,480,635 | G/A | — | uncertain significance |
| rs768993873 | 1:35,480,729 | G/A | — | uncertain significance |
| rs1641264159 | 1:35,485,003 | G/C | — | uncertain significance |
| rs139788499 | 1:35,485,062 | T/C | — | uncertain significance |
| rs143550182 | 1:35,485,128 | G/A | — | uncertain significance |
| rs138632204 | 1:35,485,152 | C/T | — | likely benign |
| rs200506387 | 1:35,485,167 | G/A | — | uncertain significance |
| rs1411981851 | 1:35,485,199 | C/A | — | uncertain significance |
| rs141291739 | 1:35,485,208 | C/G | — | benign |
| rs768036260 | 1:35,486,072 | T/A | — | likely benign |
| rs752004886 | 1:35,496,155 | T/C | — | uncertain significance |
| rs139761789 | 1:35,496,159 | C/G | — | likely benign |
| rs74780395 | 1:35,496,174 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.