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	gnomAD frequency
NM_001292063.2(OTOG):c.7867G>A (p.Asp2623Asn)	rs183470913	0.00242
NM_001292063.2(OTOG):c.7009G>C (p.Val2337Leu)	rs540794663	0.00210
NM_001292063.2(OTOG):c.8476C>T (p.Arg2826Cys)	rs191662816	0.00208

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