List of variants in gene ACTN2 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.1371C>T (p.Arg457=)	rs114008185	0.00577
NM_001103.4(ACTN2):c.1423G>A (p.Asp475Asn)	rs80257412	0.00230
NM_001103.4(ACTN2):c.1515+15C>T	rs368107695	0.00147
NM_001103.4(ACTN2):c.2076C>T (p.Ile692=)	rs144122893	0.00097
NM_001103.4(ACTN2):c.877-6G>A	rs397516585	0.00068
NM_001103.4(ACTN2):c.537-14C>T	rs577211083	0.00005
NM_001103.4(ACTN2):c.2376C>T (p.Ala792=)	rs369320952	0.00004
NM_001103.4(ACTN2):c.2676C>T (p.Ser892=)	rs397516578	0.00003
NM_001103.4(ACTN2):c.1305A>G (p.Thr435=)	rs12043223	0.00001
NM_001103.4(ACTN2):c.1857C>A (p.Pro619=)	rs1659474774	0.00001
NM_001103.4(ACTN2):c.2475C>T (p.Thr825=)	rs758805815	0.00001
NM_001103.4(ACTN2):c.1794G>C (p.Pro598=)	rs137890030

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