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Variant (rsID / SNP)

rs111033329

OTOF

rs111033329 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTOF. Location: chromosome 2, position 26,683,874. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

OTOFConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:26683874
Cytoband
2p23.3
HGVS
NM_194248.3(OTOF):c.5558G>A (p.Arg1853Gln)
Allele change
Missense_R1853Q

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 9

Public references

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