Gene entry
CLDN14
claudin 14
- Chromosome
- 21
- Cytoband
- 21q22.13
- Variants (rsID)
- 54
CLDN14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.13). Its official name is “claudin 14”. The reference table lists 54 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs219780Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 29
- rs139628442Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 29
- rs140918123Conflicting interpretationssingle nucleotide variant
- rs143797113Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 29
- rs148223897Conflicting interpretationssingle nucleotide variant
- rs149733854Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 29
- rs74315438Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 29
- rs73902533Likely benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 29
Other listed variants
- rs128494
- rs170183
- rs219757
- rs219763
- rs219769
- rs219771
- rs219775
- rs219776
- rs219781
- rs370749
- rs377239
- rs409231
- rs439888
- rs730265
- rs915750
- rs1318500
- rs2835369
- rs2835374
- rs2835378
- rs2835390
- rs2850114
- rs4816539
- rs7279128
- rs16994180
- rs28491626
- rs35857368
- rs55885155
- rs58865958
- rs73204270
- rs73206248
- rs73902536
- rs74276156
- rs74535100
- rs75430464
- rs77409573
- rs77704788
- rs79331558
- rs79419590
- rs80029376
- rs111425381
- rs116983832
- rs117271359
- rs117392071
- rs117421817
- rs117651866
- rs117833343
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.