C1861975[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 560363	NM_001042492.3(NF1):c.989C>A (p.Ala330Glu)	NF1 (A330E)	Single nucleotide variant (missense variant)	Cafe au lait spots, multiple	GUncertain significance
Select item 560364	NM_001042492.3(NF1):c.2800_2802del (p.Phe934del)	NF1 (F934del)	Deletion (inframe_deletion)	Cafe au lait spots, multiple	GUncertain significance