"Athena Diagnostics"[submitter] AND "MHRT"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1327794	NM_000257.4(MYH7):c.5020G>T (p.Val1674Leu)	LOC126861897, MHRT +1 more (V1674L)	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiomyopathy +2 more	GUncertain significance
Select item 43035	NM_000257.4(MYH7):c.4788G>A (p.Ser1596=)	LOC126861897, MHRT +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiomyopathy	GBenign FDA Recognized database
Select item 43020	NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys)	MHRT, MYH7 (S1491C)	Single nucleotide variant (missense variant)	Cardiomyopathy	GBenign FDA Recognized database
Select item 43019	NM_000257.4(MYH7):c.4452C>T (p.Leu1484=)	MHRT, MYH7	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiomyopathy	GBenign FDA Recognized database
Select item 43010	NM_000257.4(MYH7):c.4353+10G>A	MHRT, MYH7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 453109	NM_000257.4(MYH7):c.4294G>A (p.Val1432Ile)	MHRT, MYH7 (V1432I)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +10 more	GUncertain significance

ClinVar