Gene entry
KCNH5
potassium voltage-gated channel subfamily H member 5
- Chromosome
- 14
- Cytoband
- 14q23.2
- Variants (rsID)
- 83
KCNH5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q23.2). Its official name is “potassium voltage-gated channel subfamily H member 5”. The reference table lists 83 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs146883958Benignsingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
- rs36004050Benignsingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
Other listed variants
- rs243147
- rs1040729
- rs1387754
- rs1980561
- rs2101551
- rs2355062
- rs2355741
- rs2356100
- rs4902175
- rs4902176
- rs6573466
- rs7147349
- rs7149514
- rs7155227
- rs7156008
- rs7156115
- rs8013931
- rs8020107
- rs8020132
- rs8022090
- rs8022524
- rs10047855
- rs10129697
- rs10133092
- rs10133601
- rs10140061
- rs10450921
- rs11158453
- rs11846818
- rs12147053
- rs12184955
- rs12587142
- rs12588427
- rs12589408
- rs17100282
- rs17100325
- rs17100559
- rs17100574
- rs17100627
- rs17176715
- rs28677162
- rs61381560
- rs61994850
- rs61994854
- rs72625626
- rs72728737
- rs74649775
- rs74887231
- rs75035722
- rs75605219
- rs75870849
- rs75913874
- rs76817830
- rs77149800
- rs77973281
- rs78826087
- rs79415025
- rs79415355
- rs80233880
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.