List of variants in gene ACTN2 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.877-8C>G	rs2288601	0.77958
NM_001103.4(ACTN2):c.2610G>A (p.Ser870=)	rs12063382	0.16345
NM_001103.4(ACTN2):c.2139G>A (p.Thr713=)	rs34975493	0.03463
NM_001103.4(ACTN2):c.-22C>T	rs138279482	0.02321
NM_001103.4(ACTN2):c.1810A>G (p.Met604Val)	rs35997569	0.01914
NM_001103.4(ACTN2):c.705G>C (p.Val235=)	rs2288599	0.00749
NM_001103.4(ACTN2):c.2368-17T>C	rs78961574	0.00255
NM_001103.4(ACTN2):c.1423G>A (p.Asp475Asn)	rs80257412	0.00230
NM_001103.4(ACTN2):c.1341C>T (p.Phe447=)	rs34785693	0.00215
NM_001103.4(ACTN2):c.1657-16T>C	rs148194175	0.00095
NM_001103.4(ACTN2):c.2649G>A (p.Ala883=)	rs146426213	0.00066
NM_001103.4(ACTN2):c.546T>C (p.Asp182=)	rs34263845	0.00066
NM_001103.4(ACTN2):c.784-518del	rs11355106

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