List of variants in gene TCF20 reported as pathogenic for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001378418.1(TCF20):c.2224C>T (p.Arg742Ter)	rs1555926209
NM_001378418.1(TCF20):c.2685del (p.Arg896fs)	rs1555925903
NM_001378418.1(TCF20):c.2786_2787del (p.Lys929fs)	rs1921088321
NM_001378418.1(TCF20):c.4368del (p.Gly1457fs)	rs1555924435
NM_001378418.1(TCF20):c.5069dup (p.Pro1692fs)	rs1555923822
NM_001378418.1(TCF20):c.5719del (p.Arg1907fs)	rs1936673622

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