Variants in gene ACTG1 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.228C>T (p.Val76=)	rs143028649	0.00055
NM_001614.5(ACTG1):c.803-3T>C	rs369438865	0.00019
NM_001614.5(ACTG1):c.825C>T (p.His275=)	rs145303691	0.00017
NM_001614.5(ACTG1):c.561C>T (p.Asp187=)	rs782649322	0.00011
NM_001614.5(ACTG1):c.124-9C>T	rs376850595	0.00006
NM_001614.5(ACTG1):c.123+8G>A	rs536476533	0.00001
NM_001614.5(ACTG1):c.138C>T (p.Gly46=)	rs374907377	0.00001
NM_001614.5(ACTG1):c.642G>A (p.Glu214=)	rs782187026	0.00001
NM_001614.5(ACTG1):c.1050C>T (p.Ser350=)
NM_001614.5(ACTG1):c.630C>T (p.Arg210=)
NM_001614.5(ACTG1):c.958C>T (p.Leu320=)
NM_001614.5(ACTG1):c.985-5dup	rs782289893

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