List of variants in gene MYH10 reported as pathogenic by Laboratory of Medical Genetics (UMR_S 1112), INSERM/Strasbourg University

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001256012.3(MYH10):c.3352AAG[1] (p.Lys1119del)
NM_001256012.3(MYH10):c.4505G>C (p.Arg1502Pro)	rs755969165
NM_001256012.3(MYH10):c.4884+1G>A	rs2151813002

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