List of variants in gene MVK reported as likely pathogenic for perceptual disorders

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000431.4(MVK):c.442G>A (p.Ala148Thr)	rs104895298	0.00004
NM_000431.4(MVK):c.380C>T (p.Pro127Leu)	rs775474803	0.00001
NM_000431.4(MVK):c.794T>G (p.Leu265Arg)	rs104895316

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