Variant (rsID / SNP)

rs76838169

rs76838169 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GJB2. Location: chromosome 13, position 20,763,113. Clinical significance in the table: Benign.

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Reference-table entries

GJB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:20763113
Cytoband: 13q12.11
HGVS: NM_004004.6(GJB2):c.608T>C (p.Ile203Thr)
Allele change: Missense_I203T

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 1A

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.