Variants in gene ACTN2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_001103.4(ACTN2):c.1459T>C (p.Cys487Arg)	rs1572140109
NM_001103.4(ACTN2):c.2180T>G (p.Leu727Arg)	rs1572148902
NM_001103.4(ACTN2):c.2194_2226del (p.Ala732_Ile742del)	rs1572148914
NM_001103.4(ACTN2):c.355G>A (p.Ala119Thr)	rs727502886

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