Variants in gene NKX2-5 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_004387.4(NKX2-5):c.73C>T (p.Arg25Cys)	rs28936670	0.01082
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.237G>C (p.Pro79=)	rs72554029	0.00115
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.61G>C (p.Glu21Gln)	rs104893904	0.00073
NM_004387.4(NKX2-5):c.943G>T (p.Val315Leu)	rs201249977	0.00002
NM_004387.4(NKX2-5):c.335-311_335-303del	rs200467566

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