List of variants in gene LAMA3 reported as pathogenic by Biomedical Innovation Departament, CIEMAT

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_198129.4(LAMA3):c.6319-1G>T	rs2081155250
NM_198129.4(LAMA3):c.6348_6352delinsCTGGCAAGA (p.Glu2117fs)	rs2081156116
NM_198129.4(LAMA3):c.9856G>T (p.Ala3286Ser)	rs2082978607

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