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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 8

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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.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.632C>T (p.Pro211Leu)	rs3729754	0.00026
NM_004387.4(NKX2-5):c.809G>A (p.Cys270Tyr)	rs587782931	0.00003
NM_004387.4(NKX2-5):c.943G>T (p.Val315Leu)	rs201249977	0.00002
NM_004387.4(NKX2-5):c.111G>A (p.Leu37=)	rs746594822	0.00001
NM_004387.4(NKX2-5):c.627GCC[6] (p.Pro214dup)	rs746833511

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