List of variants in gene OTOG reported as uncertain significance by Genomic Diagnostic Laboratory, Division of Genomic Diagnostics,Children's Hospital of Philadelphia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP
NM_001277269.1(OTOG):c.7045G>C (p.Val2349Leu)	rs540794663
NM_001277269.1(OTOG):c.7903G>A (p.Asp2635Asn)	rs183470913
NM_001277269.1(OTOG):c.8512C>T (p.Arg2838Cys)	rs191662816

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