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

Submission 1 (benign) minimum review status:		Submission 1 (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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.341G>A (p.Arg114Lys)	rs139876825	0.00043
NM_001083962.2(TCF4):c.504A>G (p.Val168=)	rs370160994	0.00037
NM_001083962.2(TCF4):c.1349T>C (p.Met450Thr)	rs774283982	0.00001
NM_001083962.2(TCF4):c.1990G>A (p.Ala664Thr)	rs755332116

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