List of variants reported as uncertain significance for perceptual disorders by Miami Human Genetics, University Of Miami Miller School Of Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001145809.2(MYH14):c.526G>A (p.Ala176Thr)	rs138001307	0.00014
NM_001145809.2(MYH14):c.5380G>A (p.Gly1794Arg)
NM_001145809.2(MYH14):c.547C>T (p.Arg183Trp)

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