C3888093[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1188968	NM_001139.3(ALOX12B):c.1655-30T>C	ALOX12B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1188969	NM_001139.3(ALOX12B):c.1532+30T>C	ALOX12B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1188970	NM_001139.3(ALOX12B):c.147+59_147+60del	ALOX12B	Deletion (intron variant)	not provided +1 more	GBenign

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