Related gene-specific medical variations for Gene (Select 22854) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341153	GRCh37/hg19 1p13.3(chr1:107759675-108074669)x3	NTNG1	Copy number gain	not provided	GUncertain significance
Select item 930831	NM_001113226.3(NTNG1):c.1088-13T>A	NTNG1	Single nucleotide variant (intron variant)	See cases	GUncertain significance
Select item 91929	NM_001113226.3(NTNG1):c.689C>T (p.Ala230Val)	NTNG1 (A230V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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