Variant (rsID / SNP)

rs111033405

rs111033405 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTOF. Location: chromosome 2, position 26,688,621. Clinical significance in the table: Pathogenic.

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Reference-table entries

OTOFPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:26688621
Cytoband: 2p23.3
HGVS: NM_194248.3(OTOF):c.4718T>C (p.Ile1573Thr)
Allele change: Missense_I1573T

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 9|Rare genetic deafness|Bilateral sensorineural hearing impairment|Nonsyndromic genetic hearing loss

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.