List of variants in gene TCF4 reported as likely pathogenic by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.1486+2T>C	rs1555721921
NM_001083962.2(TCF4):c.1720A>G (p.Asn574Asp)	rs2047119736
NM_001083962.2(TCF4):c.1733G>A (p.Arg578His)	rs121909123
NM_001083962.2(TCF4):c.1772_1776delinsCT (p.Leu591_Gly592delinsPro)	rs1555710416
NM_001083962.2(TCF4):c.1811_1822del (p.Pro604_Lys607del)	rs1555710171
NM_001083962.2(TCF4):c.1816A>C (p.Thr606Pro)	rs2047096127
NM_001083962.2(TCF4):c.991-1G>A

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