Gene entry
HYDIN
HYDIN axonemal central pair apparatus protein
- Chromosome
- 16
- Cytoband
- 16q22.2
- Variants (rsID)
- 39
HYDIN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.2). Its official name is “HYDIN axonemal central pair apparatus protein”. The reference table lists 39 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs2502726Benignsingle nucleotide variantPrimary ciliary dyskinesia 5
- rs75270082Benignsingle nucleotide variant
- rs78763837Benignsingle nucleotide variantPrimary ciliary dyskinesia 5
- rs79607350Conflicting interpretationssingle nucleotide variant
- rs1774266Not classifiedsynonymous_variant
Other listed variants
- rs1018960
- rs1859088
- rs3114616
- rs6416705
- rs7194960
- rs8052351
- rs11648149
- rs71401841
- rs71403819
- rs74336841
- rs75149271
- rs76166010
- rs77069808
- rs111304988
- rs112037172
- rs114262001
- rs116160354
- rs117123941
- rs117449635
- rs117572023
- rs117764644
- rs118108478
- rs140370818
- rs143849088
- rs144727714
- rs181906954
- rs183254818
- rs201503269
- rs201522018
- rs530909950
- rs546109076
- rs546131282
- rs561581920
- rs576990253
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.