Variants in gene LAMB1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002291.3(LAMB1):c.2723T>C (p.Ile908Thr)	rs139487685	0.00121
NM_002291.3(LAMB1):c.3124G>A (p.Gly1042Ser)	rs149204722	0.00043
NM_002291.3(LAMB1):c.3481C>T (p.Arg1161Cys)	rs146018013	0.00014

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