List of variants in gene ACTN2 reported as benign for Cardiovascular phenotype

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.351T>C (p.Ile117=)	rs1341864	0.99334
NM_001103.4(ACTN2):c.378C>T (p.Asn126=)	rs1341863	0.93032
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.705G>C (p.Val235=)	rs2288599	0.00749
NM_001103.4(ACTN2):c.870G>A (p.Ala290=)	rs116464082	0.00506
NM_001103.4(ACTN2):c.1423G>A (p.Asp475Asn)	rs80257412	0.00230
NM_001103.4(ACTN2):c.1298C>T (p.Ser433Leu)	rs143749154	0.00068
NM_001103.4(ACTN2):c.1292C>T (p.Ser431Leu)	rs149846886	0.00009
NM_001103.4(ACTN2):c.2235A>G (p.Arg745=)	rs141884271	0.00004
NM_001103.4(ACTN2):c.1296_1298delinsATT (p.Ser433Leu)
NM_001103.4(ACTN2):c.1452G>C (p.Gln484His)	rs200529923

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