Variant (rsID / SNP)

rs73902533

rs73902533 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLDN14. Location: chromosome 21, position 37,849,769. Clinical significance in the table: Likely benign.

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Reference-table entries

CLDN14Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 21:37849769
Cytoband: 21q22.13
HGVS: NM_001146079.2(CLDN14):c.-82+2024G>A
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 29

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.