FAAH
fatty acid amide hydrolase
Summary
This gene encodes a protein that is responsible for the hydrolysis of a number of primary and secondary fatty acid amides, including the neuromodulatory compounds anandamide and oleamide. [provided by RefSeq, Jul 2008]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200388505 | 1:46,860,011 | T/G | regulatory region variant | — |
| rs773985381 | 1:46,860,070 | C/T | — | uncertain significance |
| rs1422537000 | 1:46,860,099 | G/C | — | uncertain significance |
| rs936672412 | 1:46,860,100 | T/C | — | uncertain significance |
| rs2522791668 | 1:46,860,114 | T/G | — | uncertain significance |
| rs1295514827 | 1:46,860,123 | C/G | — | uncertain significance |
| rs1386887767 | 1:46,860,126 | A/C | — | uncertain significance |
| rs4141964 | 1:46,865,040 | T/C | regulatory region variant | — |
| rs768817925 | 1:46,870,704 | G/A | — | uncertain significance |
| rs137933045 | 1:46,870,705 | G/A | — | benign |
| rs324420 | 1:46,870,761 | C/A | missense variant | likely benign |
| rs751268440 | 1:46,870,769 | G/C | — | uncertain significance |
| rs746348249 | 1:46,871,068 | A/C | — | uncertain significance |
| rs761243387 | 1:46,871,088 | G/A | — | likely benign |
| rs767131485 | 1:46,871,090 | C/T | — | uncertain significance |
| rs148653413 | 1:46,871,098 | G/A | — | uncertain significance |
| rs746293299 | 1:46,871,146 | G/A | — | uncertain significance |
| rs377084673 | 1:46,871,303 | T/C | — | uncertain significance |
| rs72890799 | 1:46,871,374 | C/G | — | benign |
| rs72480613 | 1:46,871,713 | G/A | — | benign |
| rs139618887 | 1:46,871,744 | G/C | — | uncertain significance |
| rs769992869 | 1:46,871,927 | G/T | — | uncertain significance |
| rs145105174 | 1:46,871,973 | G/A | — | likely benign |
| rs368235427 | 1:46,871,981 | C/A | — | uncertain significance |
| rs324419 | 1:46,871,986 | T/A | stop gained | — |
| rs764656396 | 1:46,872,000 | G/T | — | uncertain significance |
| rs1398134148 | 1:46,872,010 | C/T | — | likely benign |
| rs774930131 | 1:46,872,016 | G/A | — | likely benign |
| rs873978 | 1:46,873,903 | C/T | intron variant | — |
| rs1490208539 | 1:46,874,137 | A/T | — | uncertain significance |
| rs2148451446 | 1:46,874,180 | A/G | — | uncertain significance |
| rs1020739896 | 1:46,874,209 | C/T | — | uncertain significance |
| rs77101686 | 1:46,874,246 | C/T | — | benign |
| rs2295633 | 1:46,874,383 | A/C | — | — |
| rs772255857 | 1:46,876,131 | T/C | — | uncertain significance |
| rs74783386 | 1:46,876,488 | G/C | — | benign |
| rs78008000 | 1:46,876,529 | A/G | — | benign |
| rs77724956 | 1:46,877,284 | T/G | — | benign |
| rs148829596 | 1:46,877,320 | C/T | — | likely benign |
| rs78529632 | 1:46,877,810 | C/T | — | benign |
| rs75429705 | 1:46,877,885 | C/G | — | benign |
| rs1048770401 | 1:46,877,889 | T/C | — | likely benign |
| rs201884789 | 1:46,878,761 | A/C | — | uncertain significance |
| rs78072734 | 1:46,879,139 | G/A | — | benign |
| rs769732934 | 1:46,879,152 | G/A | — | uncertain significance |
| rs200958055 | 1:46,879,185 | T/C | — | benign |
| rs370370663 | 1:46,879,194 | C/T | — | uncertain significance |
| rs2295632 | 1:46,879,562 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.