FTH1
ferritin heavy chain 1
Summary
This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs886048429 | 11:61,731,814 | A/C | — | uncertain significance |
| rs886048430 | 11:61,732,034 | A/G | — | uncertain significance |
| rs755982610 | 11:61,732,040 | G/A | — | uncertain significance |
| rs780121825 | 11:61,732,194 | G/A | — | likely benign |
| rs111249745 | 11:61,732,226 | G/A | — | benign |
| rs367593479 | 11:61,732,237 | C/T | — | uncertain significance |
| rs371388537 | 11:61,732,265 | G/A | — | benign |
| rs11554842 | 11:61,732,269 | G/A | — | uncertain significance |
| rs146700893 | 11:61,732,295 | G/A | — | likely benign |
| rs1427136243 | 11:61,732,306 | A/C | — | uncertain significance |
| rs1167278194 | 11:61,732,309 | C/G | — | uncertain significance |
| rs1056175281 | 11:61,732,315 | T/C | — | uncertain significance |
| rs886048431 | 11:61,732,338 | T/A | — | uncertain significance |
| rs767112958 | 11:61,732,341 | T/C | — | uncertain significance |
| rs753621558 | 11:61,732,368 | A/G | — | benign |
| rs753401296 | 11:61,732,472 | T/C | — | uncertain significance |
| rs1237079690 | 11:61,732,491 | G/A | — | uncertain significance |
| rs199912260 | 11:61,732,516 | A/G | — | likely benign |
| rs41453449 | 11:61,732,853 | A/C | — | likely benign |
| rs552130899 | 11:61,732,863 | C/T | — | likely benign |
| rs2541429849 | 11:61,732,893 | A/G | — | uncertain significance |
| rs886048432 | 11:61,732,894 | G/A | — | uncertain significance |
| rs762631821 | 11:61,732,904 | A/G | — | likely benign |
| rs374301256 | 11:61,732,973 | G/A | — | likely benign |
| rs77202794 | 11:61,733,250 | G/A | — | benign |
| rs114039236 | 11:61,734,635 | G/A | — | benign |
| rs1430666382 | 11:61,734,786 | T/C | — | uncertain significance |
| rs773201278 | 11:61,734,838 | G/A | — | benign |
| rs370105090 | 11:61,734,841 | G/A | — | likely benign |
| rs753914758 | 11:61,734,847 | T/G | — | likely benign |
| rs751983239 | 11:61,734,899 | G/A | — | uncertain significance |
| rs925625825 | 11:61,734,911 | G/A | — | uncertain significance |
| rs11554856 | 11:61,735,033 | G/T | — | uncertain significance |
| rs756637953 | 11:61,735,059 | A/C | — | likely benign |
| rs387906549 | 11:61,735,061 | T/A | — | pathogenic |
| rs886048433 | 11:61,735,101 | T/C | — | uncertain significance |
| rs763318260 | 11:61,735,118 | C/T | — | uncertain significance |
| rs886048434 | 11:61,735,128 | C/T | — | uncertain significance |
| rs114778979 | 11:61,735,176 | C/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.