List of variants in gene COPB1 reported as likely pathogenic for cataract

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_001144061.2(COPB1):c.1651T>G (p.Phe551Val)	rs1850476947
NM_001144061.2(COPB1):c.957+1G>T	rs1850695885

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