List of variants in gene OTOGL reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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_001378609.3(OTOGL):c.5449C>T (p.Arg1817Ter)	rs768620276	0.00003
NM_001378609.3(OTOGL):c.1441+2T>C	rs1592613721
NM_001378609.3(OTOGL):c.4273C>T (p.Arg1425Ter)	rs564117765

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