Variants in gene LAMA1 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_005559.4(LAMA1):c.3048C>A (p.Cys1016Ter)	rs754303766
NM_005559.4(LAMA1):c.505C>T (p.Arg169Ter)	rs752872595

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