List of variants in gene CLDN19 reported as likely benign for retinal disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_148960.3(CLDN19):c.129C>T (p.Ala43=)	rs780859720	0.00002
NM_148960.3(CLDN19):c.*845C>G	rs377585440

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