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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000432.4(MYL2):c.401A>C (p.Glu134Ala)	rs143139258	0.00029
NM_000432.4(MYL2):c.403-1G>C	rs199474813	0.00004
NM_000432.4(MYL2):c.184A>T (p.Lys62Ter)	rs201728041	0.00002
NM_000432.4(MYL2):c.125G>A (p.Gly42Asp)	rs863225117	0.00001
NM_000432.4(MYL2):c.188del (p.Asn63fs)	rs1177936172
NM_000432.4(MYL2):c.431_432del (p.Pro144fs)	rs1566147422
NM_000432.4(MYL2):c.488A>G (p.Glu163Gly)	rs397516407

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