List of variants in gene RSPH4A reported as likely pathogenic by UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill

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_001010892.3(RSPH4A):c.1490dup (p.Ser498fs)	rs762267064	0.00003
NM_001010892.3(RSPH4A):c.1690del (p.Gln564fs)	rs1775758975
NM_001010892.3(RSPH4A):c.1838C>G (p.Ser613Ter)	rs1775776645

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