List of variants in gene CTNND2 reported as benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001332.4(CTNND2):c.2733G>A (p.Ala911=)	rs114692065	0.00569
NM_001332.4(CTNND2):c.-9G>A	rs367770543	0.00266
NM_001332.4(CTNND2):c.2464-5G>A	rs61755690	0.00202
NM_001332.4(CTNND2):c.656CGC[9] (p.Pro226dup)	rs557341981

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