DGAT2L6
diacylglycerol O-acyltransferase 2 like 6
Summary
This gene is a member of the diacylglycerol acyltransferase 2 family. The encoded protein is a putative acyltransferase and is most likely involved in the synthesis of di- or triacylglycerol, however its substrate specificity is currently unknown. [provided by RefSeq, Feb 2015]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs112058234 | X:69,402,599 | G/C | — | — |
| rs144188551 | X:69,419,142 | T/C | — | uncertain significance |
| rs755215698 | X:69,419,168 | T/A | — | likely benign |
| rs143519268 | X:69,419,206 | C/T | — | likely benign |
| rs150960362 | X:69,419,209 | T/C | — | likely benign |
| rs770313712 | X:69,419,226 | G/C | — | uncertain significance |
| rs199964484 | X:69,419,670 | C/T | — | uncertain significance |
| rs112865288 | X:69,419,740 | C/T | — | benign |
| rs1290144188 | X:69,420,119 | T/G | — | uncertain significance |
| rs773081664 | X:69,420,120 | G/A | — | uncertain significance |
| rs976163247 | X:69,420,171 | C/G | — | likely benign |
| rs150146010 | X:69,420,222 | C/T | — | likely benign |
| rs779045388 | X:69,420,223 | G/A | — | uncertain significance |
| rs1602694301 | X:69,420,312 | G/A | — | uncertain significance |
| rs368517131 | X:69,421,800 | A/G | — | uncertain significance |
| rs141887110 | X:69,421,848 | G/A | — | likely benign |
| rs138262705 | X:69,421,898 | A/G | — | uncertain significance |
| rs1461858181 | X:69,424,184 | G/A | — | uncertain significance |
| rs375294743 | X:69,424,191 | C/T | — | likely benign |
| rs144263829 | X:69,424,226 | C/T | — | uncertain significance |
| rs76987053 | X:69,424,238 | T/G | — | uncertain significance |
| rs193921067 | X:69,424,276 | C/A | — | uncertain significance |
| rs767833042 | X:69,424,289 | T/G | — | uncertain significance |
| rs140170619 | X:69,424,308 | G/T | — | likely benign |
| rs147349994 | X:69,424,321 | G/A | — | uncertain significance |
| rs756058858 | X:69,424,340 | C/A | — | uncertain significance |
| rs371986187 | X:69,424,348 | C/T | — | uncertain significance |
| rs139413662 | X:69,424,349 | G/A | — | uncertain significance |
| rs768688431 | X:69,424,823 | C/T | — | uncertain significance |
| rs2520795341 | X:69,424,842 | C/G | — | uncertain significance |
| rs760900505 | X:69,424,848 | G/T | — | uncertain significance |
| rs2520795514 | X:69,424,870 | C/T | — | uncertain significance |
| rs748053491 | X:69,424,920 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.