Gene entry
CLCN4
Cl-/H+ antiporter 4
- Chromosome
- X
- Cytoband
- Xp22.2
- Variants (rsID)
- 38
CLCN4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.2). Its official name is “Cl-/H+ antiporter 4”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs143437511Benignsingle nucleotide variant
- rs2106801Benignsingle nucleotide variant
- rs879255583Conflicting interpretationssingle nucleotide variantCLCN4-related disorder|Inborn genetic diseases
- rs879255591Conflicting interpretationssingle nucleotide variantCLCN4-related disorder
Other listed variants
- rs1003368
- rs1007744
- rs1061191
- rs2073938
- rs2077530
- rs2239429
- rs2239430
- rs2239937
- rs2239940
- rs2239941
- rs2240018
- rs2269815
- rs2301691
- rs4830705
- rs5933820
- rs5934795
- rs5934801
- rs5934803
- rs5934805
- rs5934809
- rs5934811
- rs5934817
- rs5978386
- rs5978388
- rs5979273
- rs5979283
- rs6640621
- rs7065191
- rs10521610
- rs16985991
- rs16998804
- rs17255432
- rs41297324
- rs41309719
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.