C2674636[trait identifier] AND "CSER _CC_NCGL, University of Washingto - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 225286	NM_000222.3(KIT):c.464C>T (p.Pro155Leu)	KIT (P155L)	Single nucleotide variant (missense variant)	Piebaldism +5 more	GConflicting classifications of pathogenicity
Select item 41604	NM_000222.3(KIT):c.821C>T (p.Thr274Met)	KIT (T274M +1 more)	Single nucleotide variant (missense variant)	Gastrointestinal stromal tumor, familial +6 more	GConflicting classifications of pathogenicity