"PreventionGenetics, part of Exact Sciences"[submitter] AND "NCR3"[gen - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050030	NM_147130.3(NCR3):c.605G>A (p.Ter202=)	NCR3	Single nucleotide variant (3 prime UTR variant +1 more)	NCR3-related disorder	GLikely benign
Select item 2656403	NM_147130.3(NCR3):c.44-3del	NCR3	Deletion (intron variant)	NCR3-related disorder +1 more	GLikely benign
Select item 2656404	NM_147130.3(NCR3):c.44-8G>A	NCR3	Single nucleotide variant (intron variant)	NCR3-related disorder +1 more	GLikely benign
Select item 3044589	NM_147130.3(NCR3):c.13C>T (p.Leu5=)	NCR3	Single nucleotide variant (synonymous variant)	NCR3-related disorder	GLikely benign

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