List of variants in gene LAMB1 reported as likely pathogenic by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002291.3(LAMB1):c.1168C>T (p.Arg390Ter)	rs140459621
NM_002291.3(LAMB1):c.2724dup (p.Gly909fs)	rs1554406255
NM_002291.3(LAMB1):c.313_314del (p.Pro105fs)	rs1352532055
NM_002291.3(LAMB1):c.809dup (p.Asn270fs)	rs1554411026

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