ClinVar Miner

List of variants in gene MYO1D reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015194.3(MYO1D):c.360G>A (p.Ala120=)	rs143314446	0.00088
NM_015194.3(MYO1D):c.408T>C (p.Asn136=)	rs142109768	0.00082

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