Variants in gene ACTN2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.893G>A (p.Arg298His)	rs142482143	0.00040
NM_001103.4(ACTN2):c.2147C>T (p.Thr716Met)	rs193922635	0.00024
NM_001103.4(ACTN2):c.1292C>T (p.Ser431Leu)	rs149846886	0.00013
NM_001103.4(ACTN2):c.2367+5G>A	rs200469353	0.00013
NM_001103.4(ACTN2):c.1108-5C>T	rs369956166	0.00002
NM_001103.4(ACTN2):c.616-3C>T	rs111464645	0.00001
NM_001103.4(ACTN2):c.-98CGCCGCC[4]	rs552471202

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