Variants in gene MYL3 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: 3

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HGVS	dbSNP
NM_000258.3(MYL3):c.170C>A (p.Ala57Asp)	rs139794067
NM_000258.3(MYL3):c.307+15C>T	rs184025552
NM_000258.3(MYL3):c.532G>A (p.Asp178Asn)	rs145520567

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