List of variants in gene ACTN2 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001103.4(ACTN2):c.2139G>A (p.Thr713=)	rs34975493	0.03463
NM_001103.4(ACTN2):c.705G>C (p.Val235=)	rs2288599	0.00749
NM_001103.4(ACTN2):c.1371C>T (p.Arg457=)	rs114008185	0.00577
NM_001103.4(ACTN2):c.870G>A (p.Ala290=)	rs116464082	0.00506
NM_001103.4(ACTN2):c.536+10C>T	rs141219516	0.00429
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.1515+15C>T	rs368107695	0.00147
NM_001103.4(ACTN2):c.441G>A (p.Ser147=)	rs150182164	0.00107
NM_001103.4(ACTN2):c.126+14C>T	rs373269478	0.00098
NM_001103.4(ACTN2):c.2076C>T (p.Ile692=)	rs144122893	0.00097
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.927C>T (p.Pro309=)	rs145411160	0.00051
NM_001103.4(ACTN2):c.1975-12C>T	rs371352710	0.00036
NM_001103.4(ACTN2):c.2601C>T (p.Pro867=)	rs147245615	0.00032
NM_001103.4(ACTN2):c.1406+8C>T	rs397516567	0.00026
NM_001103.4(ACTN2):c.615+15C>T	rs369293885	0.00014
NM_001103.4(ACTN2):c.1974+10C>T	rs368354944	0.00011
NM_001103.4(ACTN2):c.165C>T (p.Ala55=)	rs193922634	0.00009
NM_001103.4(ACTN2):c.2541G>A (p.Ala847=)	rs374278766	0.00008
NM_001103.4(ACTN2):c.1794G>A (p.Pro598=)	rs137890030	0.00006
NM_001103.4(ACTN2):c.354C>T (p.Gly118=)	rs539250948	0.00006
NM_001103.4(ACTN2):c.2235A>G (p.Arg745=)	rs141884271	0.00004
NM_001103.4(ACTN2):c.18C>T (p.Pro6=)	rs368367224	0.00003
NM_001103.4(ACTN2):c.1425C>T (p.Asp475=)	rs148223734	0.00002
NM_001103.4(ACTN2):c.1704G>A (p.Ala568=)	rs369560444
NM_001103.4(ACTN2):c.18C>A (p.Pro6=)	rs368367224
NM_001103.4(ACTN2):c.918C>T (p.Asn306=)	rs148646265

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