Variants in gene combination LOC126862757, TCF4 with conflicting interpretations reported as "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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.790-9T>C	rs373434281	0.00036
NM_001083962.2(TCF4):c.903C>T (p.Asn301=)	rs781392344	0.00003

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