List of variants in gene NKX2-5 reported as benign for not specified

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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_004387.4(NKX2-5):c.63A>G (p.Glu21=)	rs2277923	0.44081
NM_004387.4(NKX2-5):c.335-311A>T	rs3095871	0.39643
NM_004387.4(NKX2-5):c.335-307T>A	rs536213285	0.01380
NM_004387.4(NKX2-5):c.73C>T (p.Arg25Cys)	rs28936670	0.01082
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	0.00381
NM_004387.4(NKX2-5):c.606G>C (p.Leu202=)	rs3729753	0.00096
NM_004387.4(NKX2-5):c.355G>T (p.Ala119Ser)	rs137852684	0.00090
NM_004387.4(NKX2-5):c.943G>T (p.Val315Leu)	rs201249977	0.00002
NM_004387.4(NKX2-5):c.*61G>T	rs703752
NM_004387.4(NKX2-5):c.335-297del	rs763099269
NM_004387.4(NKX2-5):c.335-310dup	rs763099269
NM_004387.4(NKX2-5):c.335-311_335-303del	rs200467566

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