Variants in gene LARGE1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_133642.5(LARGE1):c.1788G>A (p.Ala596=)	rs74550830	0.00224
NM_133642.5(LARGE1):c.210C>T (p.Arg70=)	rs145048151	0.00220
NM_133642.5(LARGE1):c.1644C>T (p.Asn548=)	rs113253213	0.00174
NM_133642.5(LARGE1):c.1599C>T (p.Ile533=)	rs12627793	0.00012
NM_133642.5(LARGE1):c.2073+12G>A	rs377566674

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