List of variants in gene TCF4 reported as likely benign by Illumina Laboratory Services, Illumina

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.1923G>A (p.Glu641=)	rs76956936	0.00067
NM_001083962.2(TCF4):c.*1201C>T	rs541953475	0.00002
NM_001083962.2(TCF4):c.687C>A (p.Ser229=)	rs200800656	0.00001
NM_001083962.2(TCF4):c.2702_2704del	rs150498725
NM_001083962.2(TCF4):c.3868_3870del	rs66807288
NM_001083962.2(TCF4):c.*4061dup	rs140440103
NM_001083962.2(TCF4):c.5189_5192del	rs541061758

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