MUC22
mucin 22
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants162 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28360972 | 6:30,973,245 | T/C | — | — |
| rs180897906 | 6:30,976,135 | C/A | regulatory region variant | — |
| rs28360974 | 6:30,976,219 | G/A | regulatory region variant | — |
| rs149405105 | 6:30,976,349 | G/A | upstream gene variant | — |
| rs7739491 | 6:30,979,203 | A/C | regulatory region variant | — |
| rs12530384 | 6:30,981,655 | T/G | — | — |
| rs3869097 | 6:30,984,470 | C/A | — | — |
| rs1634726 | 6:30,985,828 | G/A | intron variant | — |
| rs1632870 | 6:30,987,987 | T/A | — | — |
| rs138708628 | 6:30,988,925 | C/T | regulatory region variant | — |
| rs35768964 | 6:30,989,747 | A/G | — | — |
| rs12529884 | 6:30,989,750 | C/G | — | — |
| rs9380210 | 6:30,990,019 | A/T | — | — |
| rs1634729 | 6:30,990,055 | T/G | — | — |
| rs62399426 | 6:30,990,147 | G/A | — | — |
| rs28894976 | 6:30,990,220 | C/A | — | — |
| rs115428009 | 6:30,990,631 | G/A | intron variant | — |
| rs9394030 | 6:30,990,776 | G/T | — | — |
| rs28360984 | 6:30,990,891 | A/G | intron variant | — |
| rs1632865 | 6:30,992,724 | T/A | — | — |
| rs1156927801 | 6:30,993,306 | A/C | — | uncertain significance |
| rs1317053555 | 6:30,993,355 | G/A | — | uncertain significance |
| rs1202998013 | 6:30,993,447 | C/T | — | uncertain significance |
| rs779593058 | 6:30,993,449 | A/G | — | uncertain significance |
| rs747791085 | 6:30,993,492 | C/A | — | uncertain significance |
| rs2539014362 | 6:30,993,560 | A/G | — | uncertain significance |
| rs1020521971 | 6:30,993,593 | G/A | — | uncertain significance |
| rs78457009 | 6:30,993,635 | A/T | missense variant | — |
| rs889467046 | 6:30,993,689 | G/T | — | uncertain significance |
| rs1470903030 | 6:30,993,732 | C/A | — | uncertain significance |
| rs769803151 | 6:30,993,795 | C/G | — | uncertain significance |
| rs9501039 | 6:30,993,808 | T/G | synonymous variant | — |
| rs776467427 | 6:30,993,819 | A/G | — | likely benign |
| rs367954552 | 6:30,993,849 | A/G | — | uncertain significance |
| rs1765300508 | 6:30,993,951 | T/C | — | uncertain significance |
| rs937199021 | 6:30,993,957 | C/T | — | uncertain significance |
| rs1007846470 | 6:30,993,995 | G/T | — | uncertain significance |
| rs1308190245 | 6:30,994,037 | A/G | — | uncertain significance |
| rs751295240 | 6:30,994,046 | A/T | — | uncertain significance |
| rs1372391635 | 6:30,994,066 | G/C | — | uncertain significance |
| rs1460410556 | 6:30,994,073 | A/G | — | uncertain significance |
| rs1266236716 | 6:30,994,079 | T/A | — | uncertain significance |
| rs1377406329 | 6:30,994,085 | G/A | — | uncertain significance |
| rs896871447 | 6:30,994,103 | A/C | — | uncertain significance |
| rs1329293909 | 6:30,994,104 | C/A | — | uncertain significance |
| rs1448315783 | 6:30,994,124 | C/G | — | uncertain significance |
| rs1765343135 | 6:30,994,143 | T/C | — | uncertain significance |
| rs1765343863 | 6:30,994,145 | T/A | — | uncertain significance |
| rs182397327 | 6:30,994,163 | A/G | — | uncertain significance |
| rs1414673491 | 6:30,994,164 | C/T | — | uncertain significance |
| rs558027735 | 6:30,994,184 | G/A | — | uncertain significance |
| rs1049090373 | 6:30,994,185 | A/G | — | uncertain significance |
| rs1286487686 | 6:30,994,217 | A/T | — | uncertain significance |
| rs2539020473 | 6:30,994,223 | A/G | — | uncertain significance |
| rs1765354930 | 6:30,994,226 | G/T | — | uncertain significance |
| rs747151271 | 6:30,994,280 | A/G | — | uncertain significance |
| rs1398282573 | 6:30,994,325 | G/A | — | uncertain significance |
| rs528393416 | 6:30,994,341 | C/A | — | uncertain significance |
| rs1158949703 | 6:30,994,359 | C/G | — | uncertain significance |
| rs201856601 | 6:30,994,365 | C/A | — | likely benign |
| rs138073256 | 6:30,994,370 | G/A | — | uncertain significance |
| rs771431224 | 6:30,994,394 | A/T | — | uncertain significance |
| rs2539022351 | 6:30,994,430 | A/G | — | uncertain significance |
| rs1352565591 | 6:30,994,530 | C/A | — | uncertain significance |
| rs546686317 | 6:30,994,563 | C/A | — | likely benign |
| rs757406932 | 6:30,994,579 | T/C | — | likely benign |
| rs747993060 | 6:30,994,592 | A/G | — | likely benign |
| rs1381908674 | 6:30,994,593 | C/A | — | uncertain significance |
| rs2539023927 | 6:30,994,626 | A/C | — | uncertain significance |
| rs575443639 | 6:30,994,671 | A/G | — | uncertain significance |
| rs1363946538 | 6:30,994,682 | G/T | — | uncertain significance |
| rs932371185 | 6:30,994,712 | G/A | — | uncertain significance |
| rs2539025097 | 6:30,994,769 | G/A | — | uncertain significance |
| rs529269315 | 6:30,994,809 | A/G | — | uncertain significance |
| rs868419299 | 6:30,994,817 | G/A | — | likely benign |
| rs550589877 | 6:30,994,841 | C/A | — | likely benign |
| rs566731348 | 6:30,994,889 | A/G | missense variant | — |
| rs1022253979 | 6:30,994,910 | G/T | — | uncertain significance |
| rs1396871290 | 6:30,994,923 | G/A | — | uncertain significance |
| rs1184355072 | 6:30,994,963 | A/C | — | likely benign |
| rs557946998 | 6:30,994,978 | C/T | — | likely benign |
| rs879124957 | 6:30,995,032 | C/G | — | likely benign |
| rs1310607082 | 6:30,995,077 | T/A | — | likely benign |
| rs567826735 | 6:30,995,098 | T/C | — | likely benign |
| rs777113772 | 6:30,995,157 | C/T | — | likely benign |
| rs1581654706 | 6:30,995,174 | A/C | — | uncertain significance |
| rs533149851 | 6:30,995,193 | A/G | — | likely benign |
| rs902550092 | 6:30,995,208 | C/T | — | uncertain significance |
| rs559797069 | 6:30,995,213 | T/C | — | uncertain significance |
| rs1028595617 | 6:30,995,277 | C/T | — | uncertain significance |
| rs1581655308 | 6:30,995,282 | G/A | — | uncertain significance |
| rs763910538 | 6:30,995,432 | G/T | — | uncertain significance |
| rs916746225 | 6:30,995,450 | G/T | — | uncertain significance |
| rs1290735900 | 6:30,995,528 | G/A | — | uncertain significance |
| rs551393096 | 6:30,995,636 | A/G | — | uncertain significance |
| rs961124509 | 6:30,995,732 | G/A | — | uncertain significance |
| rs1167613686 | 6:30,995,748 | C/T | — | uncertain significance |
| rs1765593685 | 6:30,995,781 | C/T | — | uncertain significance |
| rs1765603658 | 6:30,995,856 | C/T | — | uncertain significance |
| rs190445444 | 6:30,995,877 | C/T | — | uncertain significance |
Showing 100 of 162 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.