"Center for Statistical Genetics, Columbia University"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 981918	NM_001365951.3(KIF1B):c.2115+6005C>T	KIF1B (P689L)	Single nucleotide variant (missense variant +1 more)	Intellectual disability	GUncertain significance
Select item 981892	NM_001365951.3(KIF1B):c.2681C>T (p.Pro894Leu)	KIF1B, LOC126805614 (P848L +1 more)	Single nucleotide variant (missense variant)	Intellectual disability	GUncertain significance