List of variants in gene LAMA5 reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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_005560.6(LAMA5):c.4213G>A (p.Ala1405Thr)	rs779995373	0.00008
NM_005560.6(LAMA5):c.6148C>T (p.Arg2050Cys)	rs377244239	0.00004
NM_005560.6(LAMA5):c.7975C>T (p.Arg2659Trp)	rs201012962	0.00002

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