List of variants in gene combination CTNND1, TMX2-CTNND1 reported as benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001085458.2(CTNND1):c.1420+160A>T	rs514691	0.98978
NM_001085458.2(CTNND1):c.2639-170C>A	rs623541	0.53238
NM_001085458.2(CTNND1):c.483C>T (p.Asp161=)	rs10896644	0.33696
NM_001085458.2(CTNND1):c.2435+158A>G	rs612688	0.28279
NM_001085458.2(CTNND1):c.2243-120A>G	rs11570210	0.03697
NM_001085458.2(CTNND1):c.956+132G>T	rs11570196	0.02942
NM_001085458.2(CTNND1):c.2895+73C>T	rs11229140	0.02732
NM_001085458.2(CTNND1):c.2744G>A (p.Arg915Lys)	rs11570222	0.01181

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