Variants with conflicting interpretations "pathogenic" from Molecular Genetics Laboratory, Institute for Ophthalmic Research and "uncertain significance" from any submitter

Minimum review status of the submission from Molecular Genetics Laboratory, Institute for Ophthalmic Research:		Collection method of the submission from Molecular Genetics Laboratory, Institute for Ophthalmic Research:
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Show significances as they were submitted (without aggregation into standard terms)
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Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.1208G>A (p.Arg403Gln)	rs147876778	0.00119
NM_000883.4(IMPDH1):c.71G>C (p.Arg24Pro)	rs946898300	0.00018
NM_001142800.2(EYS):c.9392G>C (p.Gly3131Ala)	rs772888249	0.00006
NM_201548.5(CERKL):c.950G>A (p.Arg317His)	rs150587104	0.00004
NM_001297.5(CNGB1):c.2603G>A (p.Gly868Asp)	rs770961534	0.00001
NM_152618.3(BBS12):c.1504G>T (p.Ala502Ser)	rs142593414	0.00001
NM_006445.4(PRPF8):c.5803C>T (p.Arg1935Cys)	rs1911322255

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