Variants with conflicting interpretations "uncertain significance" from Ocular Genomics Institute, Massachusetts Eye and Ear and "pathogenic" from any submitter

Minimum review status of the submission from Ocular Genomics Institute, Massachusetts Eye and Ear:		Collection method of the submission from Ocular Genomics Institute, Massachusetts Eye and Ear:
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_022787.4(NMNAT1):c.634G>A (p.Val212Met)	rs201994921	0.00004
NM_206933.4(USH2A):c.9882C>G (p.Cys3294Trp)	rs749228276	0.00003
NM_001142800.2(EYS):c.2528G>A (p.Gly843Glu)	rs74419361	0.00002
NM_001142800.2(EYS):c.9061G>C (p.Ala3021Pro)	rs569561277	0.00001
NM_206933.4(USH2A):c.11156G>T (p.Arg3719Leu)	rs527236139

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