List of variants in gene MYH3 reported as uncertain significance for MYH3-Related 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002470.4(MYH3):c.1309T>A (p.Phe437Ile)	rs763091291
NM_002470.4(MYH3):c.248C>G (p.Pro83Arg)	rs199513213
NM_002470.4(MYH3):c.3593C>A (p.Ala1198Glu)
NM_002470.4(MYH3):c.3976G>C (p.Ala1326Pro)
NM_002470.4(MYH3):c.523A>C (p.Ile175Leu)	rs748140522

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