ZSWIM6
zinc finger SWIM-type containing 6
Summary
The protein encoded by this gene contains a zinc finger SWI2/SNF2 and MuDR (SWIM) domain. Proteins with SWIM domains have been found in a diverse number of species and are predicted to interact with DNA or proteins. Mutations in this gene result in acromelic frontonasal dysostosis. [provided by RefSeq, Apr 2017]
Known Variants689 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs913733220 | 5:60,628,094 | G/A | — | uncertain significance |
| rs1043448103 | 5:60,628,105 | G/A | — | likely benign |
| rs1291036973 | 5:60,628,106 | G/C | — | uncertain significance |
| rs1744263511 | 5:60,628,112 | G/A | — | uncertain significance |
| rs1444795610 | 5:60,628,114 | A/G | — | likely benign |
| rs1744263792 | 5:60,628,120 | G/A | — | likely benign |
| rs1483067522 | 5:60,628,121 | C/T | — | uncertain significance |
| rs1219369551 | 5:60,628,125 | C/T | — | uncertain significance |
| rs1744264232 | 5:60,628,127 | C/A | — | uncertain significance |
| rs943024318 | 5:60,628,128 | C/A | — | conflicting classifications of pathogenicity |
| rs1038709799 | 5:60,628,130 | G/A | — | uncertain significance |
| rs1345013612 | 5:60,628,139 | C/T | — | likely benign |
| rs1439290689 | 5:60,628,153 | G/A | — | benign |
| rs1744267178 | 5:60,628,172 | G/A | — | uncertain significance |
| rs1391335960 | 5:60,628,174 | G/C | — | likely benign |
| rs1456197449 | 5:60,628,181 | A/G | — | conflicting classifications of pathogenicity |
| rs963100061 | 5:60,628,184 | G/A | — | uncertain significance |
| rs1378024753 | 5:60,628,208 | G/A | — | uncertain significance |
| rs1228304711 | 5:60,628,217 | T/G | — | uncertain significance |
| rs1251801615 | 5:60,628,220 | G/A | — | conflicting classifications of pathogenicity |
| rs1189008336 | 5:60,628,221 | C/T | — | uncertain significance |
| rs1422977600 | 5:60,628,226 | C/G | — | uncertain significance |
| rs1744270827 | 5:60,628,228 | G/A | — | likely benign |
| rs1253791362 | 5:60,628,229 | C/G | — | uncertain significance |
| rs991997128 | 5:60,628,230 | C/T | — | uncertain significance |
| rs1483697647 | 5:60,628,235 | C/T | — | uncertain significance |
| rs913731645 | 5:60,628,236 | C/G | — | likely benign |
| rs1244678082 | 5:60,628,241 | G/A | — | uncertain significance |
| rs1579933532 | 5:60,628,244 | G/A | — | uncertain significance |
| rs945198780 | 5:60,628,254 | C/T | — | uncertain significance |
| rs2478706099 | 5:60,628,266 | C/T | — | uncertain significance |
| rs1156341429 | 5:60,628,270 | C/T | — | likely benign |
| rs571004627 | 5:60,628,273 | G/C | — | likely benign |
| rs1161891703 | 5:60,628,284 | C/G | — | uncertain significance |
| rs1385288279 | 5:60,628,306 | C/T | — | likely benign |
| rs1744274423 | 5:60,628,312 | C/T | — | likely benign |
| rs2478706314 | 5:60,628,313 | C/G | — | uncertain significance |
| rs1460862071 | 5:60,628,318 | C/T | — | likely benign |
| rs757648079 | 5:60,628,321 | C/T | — | likely benign |
| rs1224336978 | 5:60,628,328 | C/T | — | likely benign |
| rs2112012408 | 5:60,628,338 | T/C | — | uncertain significance |
| rs553592342 | 5:60,628,342 | G/T | — | likely benign |
| rs1198182243 | 5:60,628,369 | G/A | — | likely benign |
| rs1470191789 | 5:60,628,378 | C/T | — | likely benign |
| rs748105401 | 5:60,628,387 | G/A | — | likely benign |
| rs1414352823 | 5:60,628,388 | C/A | — | uncertain significance |
| rs772018109 | 5:60,628,405 | G/T | — | likely benign |
| rs75429795 | 5:60,628,411 | T/G | — | likely benign |
| rs111274143 | 5:60,628,414 | G/T | — | benign |
| rs1200766544 | 5:60,628,424 | A/G | — | uncertain significance |
| rs1170342046 | 5:60,628,429 | C/T | — | likely benign |
| rs2478706973 | 5:60,628,445 | C/T | — | uncertain significance |
| rs764639032 | 5:60,628,447 | C/T | — | likely benign |
| rs556865061 | 5:60,628,450 | C/T | — | benign |
| rs1450533686 | 5:60,628,484 | A/G | — | uncertain significance |
| rs1193439288 | 5:60,628,498 | C/A | — | likely benign |
| rs1235008491 | 5:60,628,501 | G/C | — | likely benign |
| rs2112012904 | 5:60,628,503 | G/A | — | uncertain significance |
| rs545400594 | 5:60,628,504 | C/T | — | likely benign |
| rs754658198 | 5:60,628,506 | G/T | — | uncertain significance |
| rs1744279853 | 5:60,628,512 | G/A | — | uncertain significance |
| rs1327267898 | 5:60,628,520 | A/T | — | uncertain significance |
| rs2478707363 | 5:60,628,524 | G/A | — | uncertain significance |
| rs2478707437 | 5:60,628,532 | G/T | — | uncertain significance |
| rs1342427053 | 5:60,628,540 | G/A | — | likely benign |
| rs2478707588 | 5:60,628,548 | G/C | — | uncertain significance |
| rs1419523977 | 5:60,628,549 | C/T | — | likely benign |
| rs2478707596 | 5:60,628,550 | G/T | — | uncertain significance |
| rs1430663925 | 5:60,628,559 | G/A | — | uncertain significance |
| rs2112013166 | 5:60,628,562 | T/G | — | uncertain significance |
| rs1288894654 | 5:60,628,563 | C/T | — | conflicting classifications of pathogenicity |
| rs1226331320 | 5:60,628,564 | C/T | — | likely benign |
| rs1744283691 | 5:60,628,572 | C/A | — | likely benign |
| rs1579933996 | 5:60,628,589 | G/C | — | uncertain significance |
| rs190547379 | 5:60,628,591 | G/C | — | likely benign |
| rs964738831 | 5:60,628,597 | A/G | — | likely benign |
| rs1439180609 | 5:60,628,601 | T/G | — | likely benign |
| rs2112013550 | 5:60,628,602 | C/T | — | uncertain significance |
| rs1372259660 | 5:60,628,603 | G/C | — | likely benign |
| rs1225114484 | 5:60,628,606 | C/T | — | likely benign |
| rs1160694252 | 5:60,628,609 | C/T | — | likely benign |
| rs1481566444 | 5:60,628,612 | C/T | — | likely benign |
| rs1455523258 | 5:60,628,615 | C/A | — | likely benign |
| rs1262666805 | 5:60,628,616 | G/C | — | uncertain significance |
| rs1216738054 | 5:60,628,618 | T/C | — | likely benign |
| rs867108301 | 5:60,628,621 | C/A | — | likely benign |
| rs1487005209 | 5:60,628,624 | C/T | — | likely benign |
| rs1436514875 | 5:60,628,627 | C/T | — | likely benign |
| rs1167757057 | 5:60,628,628 | G/A | — | uncertain significance |
| rs1215325430 | 5:60,628,631 | G/T | — | conflicting classifications of pathogenicity |
| rs1187393011 | 5:60,628,633 | C/T | — | likely benign |
| rs1483039307 | 5:60,628,636 | C/T | — | likely benign |
| rs2478708415 | 5:60,628,644 | C/T | — | uncertain significance |
| rs1349272122 | 5:60,628,645 | C/T | — | likely benign |
| rs1481666079 | 5:60,628,648 | C/T | — | likely benign |
| rs1744292271 | 5:60,628,650 | C/T | — | uncertain significance |
| rs1296722699 | 5:60,628,655 | G/T | — | uncertain significance |
| rs776194131 | 5:60,628,656 | C/T | — | likely benign |
| rs746876878 | 5:60,628,681 | C/T | — | likely benign |
| rs1378516846 | 5:60,628,682 | G/A | — | uncertain significance |
Showing 100 of 689 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.