Variants with conflicting interpretations "uncertain significance" from Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago and "risk factor" from any submitter

Minimum review status of the submission from Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago:		Collection method of the submission from Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_182919.4(TICAM1):c.1702G>A (p.Ala568Thr)	rs143679494	0.00269

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