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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002291.3(LAMB1):c.476C>G (p.Thr159Ser)	rs140146478	0.00233
NM_002291.3(LAMB1):c.1945G>A (p.Asp649Asn)	rs142386151	0.00147
NM_002291.3(LAMB1):c.1736G>A (p.Arg579Gln)	rs115518856	0.00126
NM_002291.3(LAMB1):c.3038G>A (p.Arg1013Gln)	rs141390544	0.00054
NM_002291.3(LAMB1):c.3124G>A (p.Gly1042Ser)	rs149204722	0.00043
NM_002291.3(LAMB1):c.2152G>A (p.Val718Met)	rs142742847	0.00022
NM_002291.3(LAMB1):c.1447C>T (p.Arg483Cys)	rs139568495	0.00015
NM_002291.3(LAMB1):c.4746-3C>A	rs200654865	0.00012
NM_002291.3(LAMB1):c.5225-8C>A	rs778153007	0.00009
NM_002291.3(LAMB1):c.3391+4A>C	rs766051911	0.00004
NM_002291.3(LAMB1):c.1422C>G (p.Ser474=)	rs780369106
NM_002291.3(LAMB1):c.3077G>A (p.Arg1026Gln)	rs193010498
NM_002291.3(LAMB1):c.3947-3T>C
NM_002291.3(LAMB1):c.423+3A>G

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