ClinVar for MedGen (Select 436081) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 517646	NM_000899.5(KITLG):c.130-11dup	KITLG	Duplication (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 12812	NC_000012.12:g.88905969C>T	KITLG	Single nucleotide variant	SKIN/HAIR/EYE PIGMENTATION 7, DARK/LIGHT SKIN	GAffects
Select item 12811	NC_000012.12:g.88934558T>C	KITLG	Single nucleotide variant	SKIN/HAIR/EYE PIGMENTATION 7, DARK/LIGHT SKIN	GAffects

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