List of variants in gene ACTN2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 10

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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.1296G>A (p.Ala432=)	rs35956798	0.04366
NM_001103.4(ACTN2):c.2139G>A (p.Thr713=)	rs34975493	0.03463
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.1932C>A (p.Ala644=)	rs144680712	0.00314
NM_001103.4(ACTN2):c.1341C>T (p.Phe447=)	rs34785693	0.00215
NM_001103.4(ACTN2):c.1298C>T (p.Ser433Leu)	rs143749154	0.00068
NM_001103.4(ACTN2):c.546T>C (p.Asp182=)	rs34263845	0.00066

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