List of variants in gene NKX2-5 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004387.4(NKX2-5):c.63A>G (p.Glu21=)	rs2277923	0.44069
NM_004387.4(NKX2-5):c.861C>T (p.Ala287=)	rs77612903	0.00681
NM_004387.4(NKX2-5):c.543G>A (p.Gln181=)	rs72554028	0.00578
NM_004387.4(NKX2-5):c.594G>A (p.Gln198=)	rs7728764	0.00355
NM_004387.4(NKX2-5):c.237G>C (p.Pro79=)	rs72554029	0.00115
NM_004387.4(NKX2-5):c.335-310dup	rs763099269
NM_004387.4(NKX2-5):c.335-311_335-303del	rs200467566

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