List of variants in gene TCF7L2 reported as pathogenic by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001367943.1(TCF7L2):c.1144C>T (p.Gln382Ter)	rs2137155220
NM_001367943.1(TCF7L2):c.1219C>T (p.Arg407Ter)	rs2137179429
NM_001367943.1(TCF7L2):c.1258C>T (p.Arg420Trp)
NM_001367943.1(TCF7L2):c.553-1G>A	rs2136838531

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