SLC25A37
solute carrier family 25 member 37
Summary
SLC25A37 is a solute carrier localized in the mitochondrial inner membrane. It functions as an essential iron importer for the synthesis of mitochondrial heme and iron-sulfur clusters (summary by Chen et al., 2009 [PubMed 19805291]).[supplied by OMIM, Jan 2011]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74790254 | 8:23,385,228 | G/C | regulatory region variant | — |
| rs761026684 | 8:23,386,561 | A/G | — | uncertain significance |
| rs2486896128 | 8:23,386,606 | A/T | — | uncertain significance |
| rs560257641 | 8:23,386,639 | A/G | — | uncertain significance |
| rs774625163 | 8:23,386,640 | G/C | — | uncertain significance |
| rs2486896341 | 8:23,386,643 | C/G | — | uncertain significance |
| rs1801609564 | 8:23,386,716 | C/G | — | uncertain significance |
| rs17089329 | 8:23,390,046 | C/G | regulatory region variant | — |
| rs3736030 | 8:23,392,733 | C/T | intron variant | — |
| rs952825245 | 8:23,395,042 | C/T | — | — |
| rs7842120 | 8:23,396,830 | T/A | — | — |
| rs7842144 | 8:23,396,874 | T/G | regulatory region variant | — |
| rs10098103 | 8:23,397,081 | T/C | intron variant | — |
| rs11785620 | 8:23,398,955 | T/A | regulatory region variant | — |
| rs12549025 | 8:23,399,537 | A/G | regulatory region variant | — |
| rs12549572 | 8:23,399,644 | T/C | regulatory region variant | — |
| rs201643157 | 8:23,399,890 | C/T | — | — |
| rs6557682 | 8:23,399,965 | T/C | intron variant | — |
| rs62503324 | 8:23,400,615 | C/T | intron variant | — |
| rs11783469 | 8:23,401,395 | C/T | intron variant | — |
| rs11778247 | 8:23,403,378 | G/A | intron variant | — |
| rs2872717 | 8:23,403,424 | T/A | — | — |
| rs139588299 | 8:23,403,553 | C/T | intron variant | — |
| rs60392867 | 8:23,404,016 | A/G | intron variant | — |
| rs192095068 | 8:23,404,129 | G/T | — | — |
| rs7823032 | 8:23,406,534 | A/T | — | — |
| rs67632614 | 8:23,407,315 | A/G | downstream gene variant | — |
| rs2978486 | 8:23,408,508 | G/T | regulatory region variant | — |
| rs2928666 | 8:23,412,649 | T/G | — | — |
| rs11784870 | 8:23,415,524 | G/A | intron variant | — |
| rs2018490 | 8:23,416,887 | T/C | regulatory region variant | — |
| rs376704509 | 8:23,423,729 | G/A | — | uncertain significance |
| rs774399729 | 8:23,423,799 | G/A | — | uncertain significance |
| rs376194584 | 8:23,423,830 | A/G | — | likely benign |
| rs767719031 | 8:23,425,883 | C/T | — | uncertain significance |
| rs2978482 | 8:23,427,928 | G/T | — | — |
| rs1301115918 | 8:23,428,850 | G/A | — | uncertain significance |
| rs1162450042 | 8:23,428,947 | G/A | — | uncertain significance |
| rs371477159 | 8:23,428,965 | T/C | — | uncertain significance |
| rs116050502 | 8:23,429,093 | G/T | — | benign |
| rs898400813 | 8:23,429,120 | G/A | — | uncertain significance |
| rs375896705 | 8:23,429,152 | C/A | — | uncertain significance |
| rs748631726 | 8:23,429,180 | G/C | — | uncertain significance |
| rs34146184 | 8:23,429,182 | C/T | — | benign |
| rs764970288 | 8:23,429,214 | C/T | — | uncertain significance |
| rs201447306 | 8:23,429,255 | A/T | — | uncertain significance |
| rs759792762 | 8:23,429,349 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.