Gene entry
HCN1
hyperpolarization activated cyclic nucleotide gated potassium channel 1
- Chromosome
- 5
- Cytoband
- 5p12
- Variants (rsID)
- 47
HCN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p12). Its official name is “hyperpolarization activated cyclic nucleotide gated potassium channel 1”. The reference table lists 47 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs587777493Pathogenicsingle nucleotide variantDevelopmental and epileptic encephalopathy, 24
Other listed variants
- rs1501357
- rs4866929
- rs6865405
- rs9292918
- rs12513449
- rs12517615
- rs12519133
- rs12522771
- rs12659024
- rs13170143
- rs16902191
- rs34159951
- rs34835217
- rs59316994
- rs72762058
- rs74628473
- rs75558549
- rs75777478
- rs76049424
- rs76063574
- rs76651429
- rs76855774
- rs76905871
- rs77732644
- rs78052972
- rs78112135
- rs78694495
- rs79583745
- rs79683485
- rs80335816
- rs114149695
- rs114303263
- rs114510199
- rs114792089
- rs115238150
- rs116040875
- rs138959660
- rs140245876
- rs140799600
- rs140943982
- rs144362060
- rs149106380
- rs150182972
- rs185785605
- rs192447474
- rs369451404
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.