Related gene-specific medical variations for Gene (Select 100616120) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2897290	NM_003748.4(ALDH4A1):c.604-18C>T	ALDH4A1, MIR4695	Single nucleotide variant (non-coding transcript variant +1 more)	Hyperprolinemia type 2	GLikely benign
Select item 876209	NM_003748.4(ALDH4A1):c.603+14G>A	ALDH4A1, MIR4695	Single nucleotide variant (non-coding transcript variant +1 more)	Hyperprolinemia type 2 +1 more	GBenign/Likely benign