Related gene-specific medical variations for Gene (Select 55908) - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2405242	NM_018687.7(ANGPTL8):c.364G>C (p.Ala122Pro)	DOCK6, ANGPTL8 (A122P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2377621	NM_018687.7(ANGPTL8):c.215G>A (p.Arg72His)	DOCK6, ANGPTL8 (R72H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2245604	NM_018687.7(ANGPTL8):c.164C>T (p.Thr55Ile)	DOCK6, ANGPTL8 (T55I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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