Variants with conflicting interpretations "pathogenic" from Laboratory of Genetics in Ophthalmology, Institut Imagine and "uncertain significance" from any submitter

Minimum review status of the submission from Laboratory of Genetics in Ophthalmology, Institut Imagine:		Collection method of the submission from Laboratory of Genetics in Ophthalmology, Institut Imagine:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_014336.5(AIPL1):c.715T>C (p.Cys239Arg)	rs62637012
NM_020366.4(RPGRIP1):c.2367+23del	rs781728563

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