ANGPTL6
angiopoietin like 6
Summary
Predicted to enable signaling receptor binding activity. Predicted to be involved in angiogenesis; blood coagulation; and cell differentiation. Located in collagen-containing extracellular matrix and extracellular exosome. Biomarker of gestational diabetes. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375422459 | 19:10,203,315 | C/T | — | uncertain significance |
| rs45600037 | 19:10,203,362 | C/T | — | uncertain significance |
| rs2513656493 | 19:10,203,387 | C/T | — | uncertain significance |
| rs1017022114 | 19:10,204,068 | G/C | — | uncertain significance |
| rs774373722 | 19:10,204,127 | G/A | — | uncertain significance |
| rs1480689695 | 19:10,204,132 | T/G | — | uncertain significance |
| rs200296130 | 19:10,204,136 | C/T | — | uncertain significance |
| rs76783850 | 19:10,204,143 | G/A | — | benign |
| rs2088448814 | 19:10,204,171 | G/C | — | uncertain significance |
| rs147149731 | 19:10,204,175 | A/G | — | benign |
| rs747941692 | 19:10,204,184 | G/A | — | uncertain significance |
| rs367822624 | 19:10,204,228 | C/T | — | uncertain significance |
| rs758560495 | 19:10,204,282 | C/T | — | likely benign |
| rs182345321 | 19:10,204,530 | G/A | — | uncertain significance |
| rs2513661409 | 19:10,204,539 | C/T | — | uncertain significance |
| rs780461920 | 19:10,205,574 | C/T | — | uncertain significance |
| rs2145172249 | 19:10,206,738 | C/T | — | uncertain significance |
| rs1271967962 | 19:10,206,747 | G/A | — | uncertain significance |
| rs778278866 | 19:10,206,794 | T/G | — | uncertain significance |
| rs779899913 | 19:10,206,801 | A/G | — | uncertain significance |
| rs772714067 | 19:10,206,814 | G/A | — | likely benign |
| rs754807990 | 19:10,206,836 | G/C | — | uncertain significance |
| rs576667683 | 19:10,206,848 | T/A | — | likely benign |
| rs537796826 | 19:10,206,858 | G/C | — | uncertain significance |
| rs1383217858 | 19:10,206,869 | G/A | — | uncertain significance |
| rs1049826545 | 19:10,206,871 | G/C | — | likely benign |
| rs962169966 | 19:10,206,935 | C/T | — | uncertain significance |
| rs994094830 | 19:10,206,939 | G/C | — | uncertain significance |
| rs1027901695 | 19:10,206,941 | C/T | — | uncertain significance |
| rs559282550 | 19:10,206,953 | A/G | — | benign |
| rs1485473683 | 19:10,207,008 | C/G | — | uncertain significance |
| rs932520115 | 19:10,207,010 | C/T | — | uncertain significance |
| rs1036720141 | 19:10,207,035 | C/G | — | uncertain significance |
| rs1270063292 | 19:10,207,047 | G/T | — | uncertain significance |
| rs2088543547 | 19:10,207,088 | C/T | — | uncertain significance |
| rs1238552502 | 19:10,207,169 | G/T | — | uncertain significance |
| rs751565560 | 19:10,207,225 | C/T | — | likely benign |
| rs11671983 | 19:10,209,192 | G/C | intron variant | — |
| rs8112063 | 19:10,209,711 | C/T | regulatory region variant | — |
| rs539432790 | 19:10,212,299 | C/G | — | — |
| rs8109578 | 19:10,213,154 | G/A | regulatory region variant | — |
| rs6511435 | 19:10,214,492 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.