Variants in gene RPE65 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_000329.3(RPE65):c.1301C>T (p.Ala434Val)	rs34627040	0.02403
NM_000329.3(RPE65):c.1155G>A (p.Thr385=)	rs62653014	0.00481
NM_000329.3(RPE65):c.881A>C (p.Lys294Thr)	rs61752901	0.00232
NM_000329.3(RPE65):c.978G>T (p.Val326=)	rs61752907	0.00186
NM_000329.3(RPE65):c.394G>A (p.Ala132Thr)	rs61752878	0.00103
NM_000329.3(RPE65):c.1244-5C>T	rs202185816	0.00074
NM_000329.3(RPE65):c.48T>C (p.Phe16=)	rs62642581	0.00059
NM_000329.3(RPE65):c.963T>G (p.Asn321Lys)	rs149916178	0.00054
NM_000329.3(RPE65):c.441A>G (p.Thr147=)	rs185049543	0.00012
NM_000329.3(RPE65):c.585C>T (p.Cys195=)	rs571111378	0.00007
NM_000329.3(RPE65):c.1302G>A (p.Ala434=)	rs62636301
NM_000329.3(RPE65):c.1302G>C (p.Ala434=)	rs62636301

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