HDHD5
haloacid dehalogenase like hydrolase domain containing 5
Summary
Predicted to be involved in glycerophospholipid biosynthetic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35327402 | 22:17,618,937 | G/A | — | likely benign |
| rs751646054 | 22:17,618,946 | G/C | — | uncertain significance |
| rs199543754 | 22:17,618,964 | C/T | — | uncertain significance |
| rs2517203873 | 22:17,618,981 | G/A | — | uncertain significance |
| rs200356314 | 22:17,619,023 | C/T | — | uncertain significance |
| rs1022815213 | 22:17,619,033 | G/C | — | uncertain significance |
| rs145080495 | 22:17,619,062 | G/A | — | uncertain significance |
| rs16982020 | 22:17,619,076 | C/G | — | benign |
| rs745396956 | 22:17,619,081 | G/T | — | uncertain significance |
| rs781249350 | 22:17,619,156 | C/T | — | uncertain significance |
| rs1357078784 | 22:17,619,215 | T/G | — | uncertain significance |
| rs142416632 | 22:17,619,228 | C/T | — | likely benign |
| rs201704251 | 22:17,619,449 | T/C | — | uncertain significance |
| rs769003367 | 22:17,619,477 | C/T | — | uncertain significance |
| rs151288224 | 22:17,619,517 | C/G | — | uncertain significance |
| rs2517206731 | 22:17,619,567 | C/G | — | uncertain significance |
| rs750756548 | 22:17,619,614 | G/A | — | uncertain significance |
| rs753038439 | 22:17,620,235 | T/A | — | — |
| rs35702540 | 22:17,622,001 | C/T | — | benign |
| rs189326179 | 22:17,622,097 | G/A | — | uncertain significance |
| rs2517214495 | 22:17,622,108 | C/G | — | uncertain significance |
| rs534899127 | 22:17,625,574 | A/G | — | — |
| rs199989327 | 22:17,625,928 | G/A | — | uncertain significance |
| rs371956696 | 22:17,625,931 | G/A | — | uncertain significance |
| rs768335992 | 22:17,625,946 | T/C | — | uncertain significance |
| rs369297006 | 22:17,625,995 | T/C | — | likely benign |
| rs746035661 | 22:17,625,996 | C/T | — | likely benign |
| rs759011167 | 22:17,629,354 | T/A | — | uncertain significance |
| rs193274952 | 22:17,629,357 | C/T | — | uncertain significance |
| rs200337729 | 22:17,630,434 | C/T | — | likely benign |
| rs200633672 | 22:17,630,459 | C/G | — | uncertain significance |
| rs754910177 | 22:17,630,560 | G/C | — | uncertain significance |
| rs2517238690 | 22:17,630,565 | G/A | — | uncertain significance |
| rs763137033 | 22:17,630,587 | G/A | — | uncertain significance |
| rs138401397 | 22:17,633,231 | A/C | intron variant | — |
| rs113824702 | 22:17,638,316 | T/C | upstream gene variant | — |
| rs773471009 | 22:17,640,054 | G/C | — | uncertain significance |
| rs2061839169 | 22:17,640,059 | T/G | — | uncertain significance |
| rs2061839789 | 22:17,640,086 | C/T | — | uncertain significance |
| rs1028162017 | 22:17,640,092 | C/G | — | uncertain significance |
| rs1276368053 | 22:17,640,096 | G/A | — | uncertain significance |
| rs986214161 | 22:17,640,125 | C/A | — | uncertain significance |
| rs1235273574 | 22:17,640,126 | A/G | — | uncertain significance |
| rs2517255462 | 22:17,640,137 | G/A | — | uncertain significance |
| rs767161718 | 22:17,640,138 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.