Variants in gene TCF4 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.1741G>T (p.Val581Phe)	rs587784460
NM_001083962.2(TCF4):c.1744C>T (p.Arg582Cys)	rs2047109965
NM_001083962.2(TCF4):c.1774G>A (p.Gly592Ser)	rs751190049
NM_001243226.3(TCF4):c.74del (p.Asn25fs)	rs752700752

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