CEACAM21
CEA cell adhesion molecule 21
Summary
Predicted to be involved in T cell activation and immune response. Predicted to be located in membrane. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs190695918 | 19:42,055,140 | T/G | upstream gene variant | — |
| rs181602484 | 19:42,056,625 | A/C | intron variant | — |
| rs2317314 | 19:42,062,307 | C/T | downstream gene variant | — |
| rs117885150 | 19:42,062,986 | C/T | — | — |
| rs4803480 | 19:42,066,279 | A/C | — | — |
| rs74727575 | 19:42,078,907 | C/T | upstream gene variant | — |
| rs79174422 | 19:42,078,934 | G/A | upstream gene variant | — |
| rs56265953 | 19:42,080,434 | A/G | upstream gene variant | — |
| rs782429214 | 19:42,082,633 | C/A | — | uncertain significance |
| rs1555791014 | 19:42,082,688 | C/T | — | likely benign |
| rs199801483 | 19:42,083,552 | C/T | — | uncertain significance |
| rs781969000 | 19:42,083,578 | C/T | — | uncertain significance |
| rs781911443 | 19:42,083,692 | A/C | — | uncertain significance |
| rs782623883 | 19:42,083,714 | A/G | — | uncertain significance |
| rs201739588 | 19:42,083,749 | G/A | — | uncertain significance |
| rs782767735 | 19:42,083,902 | C/T | — | uncertain significance |
| rs782563940 | 19:42,085,793 | C/T | — | uncertain significance |
| rs368535219 | 19:42,085,828 | C/T | — | uncertain significance |
| rs1486218161 | 19:42,085,832 | T/G | — | uncertain significance |
| rs1470888010 | 19:42,085,889 | C/A | — | uncertain significance |
| rs117018512 | 19:42,086,745 | A/C | intron variant | — |
| rs564869760 | 19:42,087,312 | A/T | — | — |
| rs117813662 | 19:42,089,924 | A/G | intron variant | — |
| rs782753932 | 19:42,090,711 | A/G | — | uncertain significance |
| rs200587219 | 19:42,090,732 | G/C | — | uncertain significance |
| rs543917314 | 19:42,091,270 | G/A | — | — |
| rs374431132 | 19:42,091,803 | G/A | — | uncertain significance |
| rs2513652981 | 19:42,091,830 | C/T | — | uncertain significance |
| rs781798147 | 19:42,091,833 | C/A | — | uncertain significance |
| rs202052341 | 19:42,091,847 | C/T | — | likely benign |
| rs782238806 | 19:42,092,205 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.