List of variants in gene NKX2-2 reported as uncertain significance for Inborn genetic diseases

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002509.4(NKX2-2):c.688G>A (p.Ala230Thr)	rs375070916	0.00009
NM_002509.4(NKX2-2):c.781A>G (p.Thr261Ala)	rs746462849	0.00009
NM_002509.4(NKX2-2):c.223C>A (p.Arg75Ser)	rs372549681	0.00003
NM_002509.4(NKX2-2):c.266G>A (p.Gly89Asp)	rs1980475888

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