Variants in gene CRB1 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.2506C>A (p.Pro836Thr)	rs116471343	0.00096
NM_201253.3(CRB1):c.135C>G (p.Cys45Trp)	rs145141811	0.00035
NM_201253.3(CRB1):c.2308G>A (p.Gly770Ser)	rs767648174	0.00003
NM_201253.3(CRB1):c.1892A>G (p.Tyr631Cys)	rs1271816211	0.00001
NM_201253.3(CRB1):c.2833G>A (p.Gly945Arg)	rs749746650	0.00001
NM_201253.3(CRB1):c.3936C>G (p.Cys1312Trp)	rs1665481687	0.00001
NM_201253.3(CRB1):c.4006-10A>G	rs766850702	0.00001
NM_201253.3(CRB1):c.1006T>C (p.Cys336Arg)	rs878853370
NM_201253.3(CRB1):c.1712A>C (p.Glu571Ala)	rs773233587
NM_201253.3(CRB1):c.1760G>A (p.Cys587Tyr)	rs1471328495
NM_201253.3(CRB1):c.2056C>T (p.Arg686Cys)	rs1204363918
NM_201253.3(CRB1):c.2365_2367del (p.Asn789del)	rs1433518605
NM_201253.3(CRB1):c.3653G>A (p.Cys1218Tyr)	rs1450635782
NM_201253.3(CRB1):c.498_506del (p.Ile167_Gly169del)	rs398124615

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