"PreventionGenetics, part of Exact Sciences"[submitter] AND "MYOZ2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 45788	NM_016599.5(MYOZ2):c.76+10A>G	MYOZ2	Single nucleotide variant (intron variant)	not specified +2 more	GLikely benign
Select item 953637	NM_016599.5(MYOZ2):c.182G>A (p.Arg61His)	MYOZ2 (R61H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +1 more	GUncertain significance
Select item 383430	NM_016599.5(MYOZ2):c.228A>G (p.Gln76=)	MYOZ2	Single nucleotide variant (synonymous variant)	MYOZ2-related disorder +4 more	GBenign/Likely benign
Select item 31788	NM_016599.5(MYOZ2):c.237A>G (p.Ala79=)	MYOZ2	Single nucleotide variant (synonymous variant)	MYOZ2-related disorder +6 more	GBenign
Select item 219286	NM_016599.5(MYOZ2):c.247-3C>T	MYOZ2	Single nucleotide variant (intron variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 45787	NM_016599.5(MYOZ2):c.750C>T (p.Thr250=)	MYOZ2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GBenign

ClinVar