"University of Washington Center for Mendelian Genomics, University of - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619598	NM_005560.6(LAMA5):c.7975C>T (p.Arg2659Trp)	LAMA5 (R2659W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1184837	NM_005560.6(LAMA5):c.6148C>T (p.Arg2050Cys)	LAMA5 (R2050C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1184836	NM_005560.6(LAMA5):c.4213G>A (p.Ala1405Thr)	LAMA5 (A1405T)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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