ClinVar Miner

List of variants in gene combination MYH8, MYHAS reported as uncertain significance by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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_002472.3(MYH8):c.2172-4G>T	rs1016250383	0.00001
NM_002472.3(MYH8):c.5665G>C (p.Glu1889Gln)	rs2508003821

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