Variants in gene ACTG1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.1003C>T (p.Arg335Cys)	rs1568060200
NM_001614.5(ACTG1):c.1004G>A (p.Arg335His)	rs1555666392
NM_001614.5(ACTG1):c.359C>T (p.Thr120Ile)	rs281875325
NM_001614.5(ACTG1):c.721G>A (p.Glu241Lys)	rs267606631
NM_001614.5(ACTG1):c.760C>T (p.Arg254Trp)	rs281875328

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