List of variants in gene NKX2-5 reported as benign by GeneDx

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: 15

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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.335-315A>T	rs55880439	0.39924
NM_004387.4(NKX2-5):c.335-311A>T	rs3095871	0.39643
NM_004387.4(NKX2-5):c.335-323A>T	rs56265301	0.06897
NM_004387.4(NKX2-5):c.334+209_334+212dup	rs35204361	0.02165
NM_004387.4(NKX2-5):c.-106A>G	rs77083308	0.01589
NC_000005.10:g.173235574C>A	rs73317175	0.01483
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.*61G>T	rs703752
NM_004387.4(NKX2-5):c.335-682G>C	rs3131915

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