MAN2B2
mannosidase alpha class 2B member 2
Summary
Predicted to enable alpha-mannosidase activity. Predicted to be involved in mannose metabolic process and oligosaccharide catabolic process. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants144 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs572704946 | 4:6,575,584 | G/A | — | — |
| rs73209743 | 4:6,576,367 | C/T | regulatory region variant | — |
| rs374156683 | 4:6,576,959 | C/T | — | uncertain significance |
| rs770090735 | 4:6,576,974 | C/T | — | uncertain significance |
| rs1226757941 | 4:6,576,983 | C/A | — | uncertain significance |
| rs762352744 | 4:6,577,020 | G/A | — | likely benign |
| rs754397390 | 4:6,577,043 | C/T | — | uncertain significance |
| rs200406024 | 4:6,577,049 | G/A | — | uncertain significance |
| rs777770254 | 4:6,577,053 | T/G | — | uncertain significance |
| rs376407727 | 4:6,577,061 | G/A | — | uncertain significance |
| rs890500719 | 4:6,577,071 | T/C | — | uncertain significance |
| rs536839038 | 4:6,577,076 | G/A | — | uncertain significance |
| rs377048827 | 4:6,578,315 | G/A | — | likely benign |
| rs368885291 | 4:6,578,323 | G/A | — | uncertain significance |
| rs145563570 | 4:6,578,326 | G/A | — | uncertain significance |
| rs1183732724 | 4:6,578,443 | A/C | — | uncertain significance |
| rs4689485 | 4:6,578,487 | A/G | — | benign |
| rs148239848 | 4:6,580,153 | T/C | — | uncertain significance |
| rs764303773 | 4:6,580,159 | A/G | — | uncertain significance |
| rs3764809 | 4:6,580,283 | G/A | — | benign |
| rs561463745 | 4:6,581,431 | C/A | — | — |
| rs139424044 | 4:6,588,384 | G/A | intron variant | — |
| rs539848113 | 4:6,588,731 | G/A | — | uncertain significance |
| rs753497334 | 4:6,588,822 | C/A | — | uncertain significance |
| rs771068415 | 4:6,588,837 | A/G | — | uncertain significance |
| rs140227562 | 4:6,588,852 | C/T | — | uncertain significance |
| rs781181349 | 4:6,588,882 | T/C | — | uncertain significance |
| rs1490806539 | 4:6,588,891 | C/T | — | uncertain significance |
| rs567854068 | 4:6,590,830 | C/T | — | uncertain significance |
| rs142352794 | 4:6,590,839 | T/C | — | uncertain significance |
| rs571316887 | 4:6,593,025 | A/C | — | — |
| rs10937747 | 4:6,594,827 | A/G | — | benign |
| rs368833584 | 4:6,594,923 | T/C | — | uncertain significance |
| rs2301796 | 4:6,594,947 | A/C | — | likely benign |
| rs140896144 | 4:6,594,971 | G/C | — | uncertain significance |
| rs138594946 | 4:6,595,027 | G/A | — | uncertain significance |
| rs769800406 | 4:6,595,051 | C/T | — | uncertain significance |
| rs766523329 | 4:6,595,059 | G/A | — | likely benign |
| rs144381772 | 4:6,595,354 | G/A | intron variant | — |
| rs370689615 | 4:6,596,289 | C/T | — | uncertain significance |
| rs149674807 | 4:6,596,307 | T/A | — | uncertain significance |
| rs143506254 | 4:6,596,345 | G/A | — | uncertain significance |
| rs2301795 | 4:6,596,360 | G/A | — | likely benign |
| rs772632113 | 4:6,596,390 | C/T | — | uncertain significance |
| rs760167740 | 4:6,596,391 | G/A | — | uncertain significance |
| rs758431473 | 4:6,596,402 | G/A | — | uncertain significance |
| rs1287834954 | 4:6,596,420 | C/T | — | uncertain significance |
| rs2301794 | 4:6,596,476 | G/A | — | benign |
| rs4234761 | 4:6,596,515 | C/T | — | benign |
| rs2301793 | 4:6,596,552 | T/C | — | benign |
| rs369552108 | 4:6,598,842 | C/T | — | uncertain significance |
| rs149837053 | 4:6,598,852 | C/T | — | uncertain significance |
| rs2548913465 | 4:6,598,863 | T/G | — | uncertain significance |
| rs375847435 | 4:6,598,900 | G/A | — | uncertain significance |
| rs144033191 | 4:6,598,903 | G/T | — | uncertain significance |
| rs778269787 | 4:6,598,945 | G/A | — | uncertain significance |
| rs902830326 | 4:6,598,960 | C/A | — | uncertain significance |
| rs149128378 | 4:6,598,963 | C/T | — | uncertain significance |
| rs771925392 | 4:6,598,966 | G/A | — | likely benign |
| rs2548913611 | 4:6,598,998 | C/A | — | uncertain significance |
| rs372236715 | 4:6,599,013 | C/T | — | uncertain significance |
| rs764591691 | 4:6,599,014 | G/A | — | uncertain significance |
| rs778484022 | 4:6,599,028 | G/A | — | uncertain significance |
| rs73209757 | 4:6,599,928 | C/A | missense variant | — |
| rs2548914167 | 4:6,599,931 | C/T | — | uncertain significance |
| rs1392253753 | 4:6,599,958 | T/A | — | uncertain significance |
| rs1436961512 | 4:6,599,959 | C/T | — | uncertain significance |
| rs2301790 | 4:6,600,012 | A/G | — | likely benign |
| rs149169745 | 4:6,600,015 | C/G | — | uncertain significance |
| rs2301789 | 4:6,602,255 | A/G | — | benign |
| rs148386673 | 4:6,602,402 | G/A | — | likely benign |
| rs755001899 | 4:6,602,415 | G/A | — | uncertain significance |
| rs2548915656 | 4:6,602,470 | C/T | — | uncertain significance |
| rs12639813 | 4:6,602,516 | A/G | — | benign |
| rs116323617 | 4:6,605,093 | G/A | intron variant | — |
| rs779234318 | 4:6,606,810 | C/T | — | uncertain significance |
| rs2548918465 | 4:6,606,812 | T/C | — | uncertain significance |
| rs774209866 | 4:6,606,855 | G/A | — | uncertain significance |
| rs2301788 | 4:6,606,864 | G/A | — | benign |
| rs61745007 | 4:6,606,907 | G/A | — | likely benign |
| rs202121114 | 4:6,606,941 | C/T | — | uncertain significance |
| rs760614382 | 4:6,606,942 | G/A | — | uncertain significance |
| rs767916354 | 4:6,606,969 | C/T | — | uncertain significance |
| rs1306754474 | 4:6,606,989 | G/A | — | uncertain significance |
| rs149325410 | 4:6,606,997 | C/T | — | likely benign |
| rs541145764 | 4:6,606,998 | G/A | — | uncertain significance |
| rs148488843 | 4:6,607,008 | T/C | — | uncertain significance |
| rs2548918765 | 4:6,607,014 | T/G | — | uncertain significance |
| rs144650979 | 4:6,607,046 | G/A | — | likely benign |
| rs573333445 | 4:6,610,609 | G/A | — | — |
| rs184138382 | 4:6,610,848 | C/T | — | uncertain significance |
| rs745775933 | 4:6,610,862 | C/T | — | likely pathogenic |
| rs768950143 | 4:6,610,883 | G/A | — | uncertain significance |
| rs2548921292 | 4:6,610,890 | G/A | — | uncertain significance |
| rs762627882 | 4:6,610,916 | G/A | — | uncertain significance |
| rs373814800 | 4:6,611,548 | C/T | — | uncertain significance |
| rs377039829 | 4:6,611,559 | C/T | — | uncertain significance |
| rs369065221 | 4:6,611,566 | G/A | — | uncertain significance |
| rs781555649 | 4:6,611,584 | A/G | — | uncertain significance |
| rs370321623 | 4:6,611,613 | C/T | — | uncertain significance |
Showing 100 of 144 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.