FAM210A family with sequence similarity 210 member A
Gene ID: 125228, updated on 14-Nov-2024Gene type: protein coding
Also known as: HsT2329; C18orf19
- See all available tests in GTR for this gene
- Go to complete Gene record for FAM210A
- Go to Variation Viewer for FAM210A variants
Summary
Located in mitochondrion. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. GeneReviews: Not available |
Genomic context
- Location:
- 18p11.21
- Sequence:
- Chromosome: 18; NC_000018.10 (13663347..13726558, complement)
- Total number of exons:
- 5
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for FAM210A variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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