List of variants in gene TCF20 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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_001378418.1(TCF20):c.2244del (p.Lys748fs)	rs2147212644
NM_001378418.1(TCF20):c.235dup (p.Tyr79fs)	rs2147223453
NM_001378418.1(TCF20):c.5570del (p.Gly1857fs)

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