List of variants in gene MVK 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000431.4(MVK):c.1128C>T (p.Gly376=)	rs147662789	0.00023
NM_000431.4(MVK):c.258G>A (p.Glu86=)	rs139299227	0.00003
NM_000431.4(MVK):c.33G>A (p.Pro11=)	rs779289416
NM_000431.4(MVK):c.384C>T (p.Ser128=)

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