Variants in gene MYL2 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.141C>A (p.Asn47Lys)	rs199474808	0.00038
NM_000432.4(MYL2):c.403-1G>C	rs199474813	0.00004
NM_000432.4(MYL2):c.119G>A (p.Arg40Lys)	rs727503299
NM_000432.4(MYL2):c.483C>A (p.His161Gln)	rs886039108

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