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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.504A>G (p.Val168=)	rs370160994	0.00037
NM_001083962.2(TCF4):c.1487-5G>A	rs749176054	0.00016
NM_001083962.2(TCF4):c.1245T>C (p.His415=)	rs148909575	0.00006
NM_001083962.2(TCF4):c.1283G>T (p.Gly428Val)	rs186508321	0.00004
NM_001083962.2(TCF4):c.1113G>A (p.Ser371=)	rs148308964	0.00003
NM_001083962.2(TCF4):c.466C>A (p.Pro156Thr)	rs200889338	0.00003
NM_001083962.2(TCF4):c.1106C>A (p.Ala369Asp)	rs1016959427	0.00001
NM_001083962.2(TCF4):c.584A>G (p.Asn195Ser)	rs148573556	0.00001
NM_001083962.2(TCF4):c.413C>G (p.Thr138Ser)	rs796053416
NM_001083962.2(TCF4):c.594G>T (p.Ser198=)	rs368553922
NM_001083962.2(TCF4):c.939G>A (p.Gly313=)	rs1470608351
NM_001083962.2(TCF4):c.990+12T>A	rs144346949

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