"NBEA-related intellectual disability"[Disease/phenotype] AND "Illumin - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 989301	NM_001385012.1(NBEA):c.539A>G (p.Asp180Gly)	NBEA (D180G)	Single nucleotide variant (missense variant)	NBEA-related intellectual disability	GUncertain significance
Select item 989302	NM_001385012.1(NBEA):c.4691C>T (p.Ala1564Val)	NBEA (A1561V +1 more)	Single nucleotide variant (missense variant)	NBEA-related intellectual disability	GUncertain significance