List of variants in gene AARS2 reported as benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_020745.4(AARS2):c.1015A>G (p.Ile339Val)	rs324136	0.89518
NM_020745.4(AARS2):c.2871A>G (p.Ser957=)	rs325008	0.88502
NM_020745.4(AARS2):c.2607G>A (p.Lys869=)	rs498512	0.67400
NM_020745.4(AARS2):c.243+6G>A	rs167772	0.50019
NM_020745.4(AARS2):c.2188G>A (p.Val730Met)	rs35623954	0.03069
NM_020745.4(AARS2):c.2548A>G (p.Met850Val)	rs35783144	0.01782
NM_020745.4(AARS2):c.2007+8C>T	rs150125794	0.00599
NM_020745.4(AARS2):c.2253G>A (p.Gly751=)	rs78397386	0.00210
NM_020745.4(AARS2):c.2679C>T (p.Leu893=)	rs766642839	0.00003

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