Variants in gene LAMC3 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.-2C>T	rs137883250	0.01424
NM_006059.4(LAMC3):c.4092C>T (p.Ser1364=)	rs141724499	0.00360
NM_006059.4(LAMC3):c.2891-8C>T	rs199535979	0.00339
NM_006059.4(LAMC3):c.2517G>A (p.Thr839=)	rs140540789	0.00292
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln)	rs146221263
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser)	rs147092908

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