List of variants in gene MYO1A reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005379.4(MYO1A):c.2021G>A (p.Gly674Asp)	rs148808080	0.00050
NM_005379.4(MYO1A):c.640+1G>C	rs199924915	0.00004
NM_005379.4(MYO1A):c.1011+2T>G	rs875989945
NM_005379.4(MYO1A):c.1882C>G (p.Arg628Gly)	rs151187460

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