Variant (rsID / SNP)

rs76461792

rs76461792 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTOG. Location: chromosome 11, position 17,656,672. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

OTOGConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 11:17656672
Cytoband: 11p15.1
HGVS: NM_001292063.2(OTOG):c.7631G>A (p.Arg2544Gln)
Allele change: Missense_R2556Q

Associated conditions / phenotypes

Meniere disease

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.