List of variants in gene MYO3A reported as likely pathogenic by Invitae

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_017433.5(MYO3A):c.2506-1G>A	rs201023600	0.00018
NM_017433.5(MYO3A):c.1563-1G>A
NM_017433.5(MYO3A):c.2793+2del
NM_017433.5(MYO3A):c.4293+1G>C
NM_017433.5(MYO3A):c.4586+2T>C	rs1843661582
NM_017433.5(MYO3A):c.508+2T>C
NM_017433.5(MYO3A):c.953+2T>C

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