List of variants in gene CHMP4B reported as likely benign 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_176812.5(CHMP4B):c.240G>A (p.Ala80=)	rs774485925	0.00003
NM_176812.5(CHMP4B):c.368+15G>A	rs199832068

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