Variants in gene CRB1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 4

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.1470C>T (p.Gly490=)	rs35193230	0.00265
NM_201253.3(CRB1):c.1647T>C (p.Asn549=)	rs62636283	0.00064
NM_201253.3(CRB1):c.2462C>T (p.Thr821Met)	rs142857810	0.00019
NM_201253.3(CRB1):c.664G>A (p.Glu222Lys)	rs114846212	0.00014

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