C5568980[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 678446	NM_002860.4(ALDH18A1):c.2207-46G>A	ALDH18A1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign
Select item 258825	NM_002860.4(ALDH18A1):c.2206+15G>A	ALDH18A1	Single nucleotide variant (intron variant)	ALDH18A1-related de Barsy syndrome +7 more	GBenign
Select item 678444	NM_002860.4(ALDH18A1):c.2110+24A>T	ALDH18A1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign
Select item 678443	NM_002860.4(ALDH18A1):c.1606-48T>G	ALDH18A1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign
Select item 258827	NM_002860.4(ALDH18A1):c.896C>T (p.Thr299Ile)	ALDH18A1 (T299I +5 more)	Single nucleotide variant (missense variant)	ALDH18A1-related de Barsy syndrome +7 more	GBenign
Select item 258826	NM_002860.4(ALDH18A1):c.304-34A>G	ALDH18A1	Single nucleotide variant (intron variant)	ALDH18A1-related de Barsy syndrome +5 more	GBenign
Select item 1188865	NM_002860.4(ALDH18A1):c.88+126A>C	ALDH18A1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign

ClinVar