Variant (rsID / SNP)

rs77835094

rs77835094 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTOGL. Location: chromosome 12, position 80,665,459. Clinical significance in the table: Benign.

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Reference-table entries

OTOGLBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:80665459
Cytoband: 12q21.31
HGVS: NM_001378609.3(OTOGL):c.2550C>T (p.Phe850=)
Allele change: Synonymous_F841F

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.