SEC14L6
SEC14 like lipid binding 6
Summary
Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2517655596 | 22:30,921,032 | C/G | — | uncertain significance |
| rs200443600 | 22:30,921,037 | C/G | — | uncertain significance |
| rs759541331 | 22:30,921,069 | C/G | — | uncertain significance |
| rs545275660 | 22:30,921,363 | A/C | — | likely benign |
| rs763007367 | 22:30,921,366 | C/A | — | uncertain significance |
| rs547797736 | 22:30,921,382 | T/C | — | uncertain significance |
| rs764125499 | 22:30,921,438 | C/T | — | uncertain significance |
| rs758826578 | 22:30,921,474 | C/T | — | uncertain significance |
| rs747938203 | 22:30,921,616 | A/G | — | uncertain significance |
| rs772014266 | 22:30,921,620 | G/T | — | uncertain significance |
| rs200755426 | 22:30,921,652 | C/T | — | uncertain significance |
| rs549859955 | 22:30,921,695 | T/C | — | uncertain significance |
| rs773725890 | 22:30,921,724 | C/G | — | uncertain significance |
| rs538834258 | 22:30,921,728 | C/A | — | uncertain significance |
| rs771434235 | 22:30,921,859 | C/T | — | uncertain significance |
| rs556275669 | 22:30,921,869 | C/T | — | likely benign |
| rs756020726 | 22:30,921,914 | A/G | — | uncertain significance |
| rs5753179 | 22:30,922,544 | T/C | intron variant | — |
| rs187122097 | 22:30,924,343 | C/T | intron variant | — |
| rs746827312 | 22:30,925,098 | G/T | — | uncertain significance |
| rs1444848482 | 22:30,925,140 | C/T | — | uncertain significance |
| rs975759810 | 22:30,925,143 | C/A | — | uncertain significance |
| rs7287003 | 22:30,925,492 | G/C | intron variant | — |
| rs35102600 | 22:30,926,321 | C/T | intron variant | — |
| rs773354534 | 22:30,928,537 | C/T | — | likely benign |
| rs2517683790 | 22:30,928,571 | T/C | — | uncertain significance |
| rs1601886919 | 22:30,928,582 | T/G | — | uncertain significance |
| rs907972107 | 22:30,928,657 | C/T | — | uncertain significance |
| rs2517685140 | 22:30,928,807 | T/C | — | uncertain significance |
| rs750682237 | 22:30,928,813 | C/G | — | uncertain significance |
| rs768715092 | 22:30,928,825 | G/T | — | uncertain significance |
| rs747632610 | 22:30,928,830 | C/T | — | uncertain significance |
| rs1937067332 | 22:30,929,995 | G/T | — | uncertain significance |
| rs1165525858 | 22:30,930,019 | G/C | — | uncertain significance |
| rs765201906 | 22:30,930,023 | C/T | — | uncertain significance |
| rs372667798 | 22:30,934,825 | C/T | — | uncertain significance |
| rs141685013 | 22:30,934,858 | G/A | — | uncertain significance |
| rs780656771 | 22:30,942,638 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.