List of variants in gene MYO5A reported as likely benign for disorder of melanin metabolism

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_001382347.1(MYO5A):c.5409+4G>A	rs72734962	0.00647
NM_001382347.1(MYO5A):c.3136G>A (p.Val1046Met)	rs56132571	0.00099
NM_001382347.1(MYO5A):c.534A>C (p.Arg178=)

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