List of variants in gene TCF3 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003200.5(TCF3):c.359T>C (p.Leu120Pro)	rs35354874	0.01928
NM_003200.5(TCF3):c.592A>G (p.Thr198Ala)	rs11879402	0.01640
NM_003200.5(TCF3):c.1062T>C (p.Ser354=)	rs11882821	0.01552
NM_003200.5(TCF3):c.302A>G (p.Lys101Arg)	rs41275842	0.00989
NM_003200.5(TCF3):c.1539C>G (p.His513Gln)	rs115383004	0.00632
NM_003200.5(TCF3):c.558A>G (p.Pro186=)	rs11879412	0.00475
NM_003200.5(TCF3):c.1713G>A (p.Glu571=)	rs143212973	0.00394
NM_003200.5(TCF3):c.-11G>C

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