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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.1165C>T (p.Arg389Cys)	rs2145503179
NM_001083962.2(TCF4):c.1169del (p.Arg389_Leu390insTer)	rs1555764839
NM_001083962.2(TCF4):c.1486+1G>T	rs2048816852
NM_001083962.2(TCF4):c.1726C>T (p.Arg576Ter)	rs1555710726
NM_001083962.2(TCF4):c.1732C>T (p.Arg578Cys)	rs2144406630
NM_001083962.2(TCF4):c.1733G>A (p.Arg578His)	rs121909123
NM_001083962.2(TCF4):c.1738C>T (p.Arg580Trp)	rs121909120
NM_001083962.2(TCF4):c.1739G>A (p.Arg580Gln)	rs121909121
NM_001083962.2(TCF4):c.1876C>T (p.Arg626Ter)	rs1131691735
NM_001083962.2(TCF4):c.1965dup (p.Gly656fs)	rs797046035
NM_001083962.2(TCF4):c.655+1G>A	rs587784465
NM_001083962.2(TCF4):c.748C>T (p.Gln250Ter)	rs727504175
NM_001083962.2(TCF4):c.990G>A (p.Ser330=)	rs587784469
Single allele

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