"Revvity Omics, Revvity"[submitter] AND "LAMA4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 851295	NM_001105206.3(LAMA4):c.5383C>T (p.His1795Tyr)	LAMA4 (H1788Y +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2433377	NM_001105206.3(LAMA4):c.3968G>A (p.Arg1323Lys)	LAMA4 (R1316K +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 650166	NM_001105206.3(LAMA4):c.2611C>T (p.Arg871Trp)	LAMA4 (R871W +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 1175087	NM_001105206.3(LAMA4):c.1176_1177insT (p.Asp393Ter)	LAMA4 (D386* +1 more)	Insertion (nonsense)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2433378	NM_001105206.3(LAMA4):c.1043G>T (p.Ser348Ile)	LAMA4 (S341I +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 213581	NM_001105206.3(LAMA4):c.829G>A (p.Val277Ile)	LAMA4 (V270I +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar