List of variants in gene TF reported as likely pathogenic for anemia

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_001063.4(TF):c.1623-63del	rs8177291	0.01085
NM_001063.4(TF):c.1444C>T (p.Pro482Ser)	rs2107925842
NM_001063.4(TF):c.1825C>T (p.Arg609Trp)	rs773139494

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