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

Minimum submission review status:		Collection method:
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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: 12

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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.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.114G>A (p.Glu38=)	rs151314714	0.00078
NM_004387.4(NKX2-5):c.61G>C (p.Glu21Gln)	rs104893904	0.00073
NM_004387.4(NKX2-5):c.492G>C (p.Ser164=)	rs754229011	0.00006
NM_004387.4(NKX2-5):c.771G>T (p.Pro257=)	rs762428190	0.00003
NM_004387.4(NKX2-5):c.583C>A (p.Arg195=)	rs960527591	0.00001
NM_004387.4(NKX2-5):c.217C>T (p.Leu73=)	rs1554093696
NM_004387.4(NKX2-5):c.334+9G>T	rs534308328
NM_004387.4(NKX2-5):c.357G>T (p.Ala119=)	rs769566306

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