List of variants in gene ACTN2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.1810A>G (p.Met604Val)	rs35997569	0.01914
NM_001103.4(ACTN2):c.1371C>T (p.Arg457=)	rs114008185	0.00577
NM_001103.4(ACTN2):c.536+10C>T	rs141219516	0.00429
NM_001103.4(ACTN2):c.1932C>A (p.Ala644=)	rs144680712	0.00314
NM_001103.4(ACTN2):c.1423G>A (p.Asp475Asn)	rs80257412	0.00230
NM_001103.4(ACTN2):c.1657-16T>C	rs148194175	0.00095
NM_001103.4(ACTN2):c.877-6G>A	rs397516585	0.00068
NM_001103.4(ACTN2):c.2649G>A (p.Ala883=)	rs146426213	0.00066
NM_001103.4(ACTN2):c.1406+8C>T	rs397516567	0.00026

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