List of variants in gene OTOF reported as uncertain significance by Division of Human Genetics, 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_194248.3(OTOF):c.154G>A (p.Val52Met)	rs199992845	0.00026
NM_194248.3(OTOF):c.2034_2042dup (p.676_678AGD[3])	rs794729640
NM_194248.3(OTOF):c.5938G>T (p.Ala1980Ser)	rs62640381

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