"PreventionGenetics, part of Exact Sciences"[submitter] AND "TCF7L2"[g - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3048632	NM_001367943.1(TCF7L2):c.296C>A (p.Pro99Gln)	TCF7L2 (P99Q)	Single nucleotide variant (missense variant)	TCF7L2-related disorder	GUncertain significance
Select item 2221608	NM_001367943.1(TCF7L2):c.451-6C>T	TCF7L2	Single nucleotide variant (intron variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 3037224	NM_001367943.1(TCF7L2):c.528G>A (p.Arg176=)	TCF7L2	Single nucleotide variant (synonymous variant +1 more)	TCF7L2-related disorder	GLikely benign
Select item 720055	NM_001367943.1(TCF7L2):c.702G>A (p.Pro234=)	TCF7L2	Single nucleotide variant (synonymous variant)	TCF7L2-related disorder +1 more	GLikely benign
Select item 3054967	NM_001367943.1(TCF7L2):c.1254C>T (p.Ser418=)	TCF7L2	Single nucleotide variant (synonymous variant)	TCF7L2-related disorder	GLikely benign
Select item 3059087	NM_001367943.1(TCF7L2):c.1570G>A (p.Ala524Thr)	TCF7L2 (A484T +3 more)	Single nucleotide variant (missense variant +1 more)	TCF7L2-related disorder	GBenign
Select item 2640844	NM_001367943.1(TCF7L2):c.1653G>A (p.Pro551=)	TCF7L2	Single nucleotide variant (synonymous variant +1 more)	TCF7L2-related disorder +1 more	GLikely benign
Select item 3058255	NM_001367943.1(TCF7L2):c.1680C>T (p.Ala560=)	TCF7L2	Single nucleotide variant (synonymous variant +1 more)	TCF7L2-related disorder	GLikely benign
Select item 741522	NM_001367943.1(TCF7L2):c.1744C>A (p.Pro582Thr)	TCF7L2 (P559T +3 more)	Single nucleotide variant (missense variant +1 more)	TCF7L2-related disorder +2 more	GBenign/Likely benign