List of variants in gene MYH3 reported as pathogenic for bone development disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002470.4(MYH3):c.-9+1G>A	rs557849165	0.00117
NM_002470.4(MYH3):c.1581+1G>A	rs1350968647	0.00001
NM_002470.4(MYH3):c.1411-391_1411-219del	rs1567558314
NM_002470.4(MYH3):c.141T>G (p.Tyr47Ter)	rs1567564042
NM_002470.4(MYH3):c.1986_1990del (p.Asn662fs)	rs771300756
NM_002470.4(MYH3):c.4647+1G>A	rs1567552713

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