List of variants in gene TBX1 reported as not provided for syndrome caused by partial chromosomal deletion

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001379200.1(TBX1):c.186C>A (p.Cys62Ter)	rs2145827917
NM_001379200.1(TBX1):c.623C>T (p.Ser208Leu)	rs1936759742
NM_080646.2(TBX1):c.1143_1149delinsTGGGTATTG (p.Phe382fs)

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