"Blueprint Genetics"[submitter] AND "DOCK2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 578432	NM_004946.3(DOCK2):c.286T>C (p.Trp96Arg)	DOCK2 (W96R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 636900	NM_004946.3(DOCK2):c.856A>T (p.Lys286Ter)	DOCK2, LOC126807589 (K286*)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 571091	NM_004946.3(DOCK2):c.1742C>T (p.Thr581Met)	DOCK2 (T581M)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 636342	NM_004946.3(DOCK2):c.2267+3G>A	DOCK2	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 636370	NM_004946.3(DOCK2):c.3599G>A (p.Arg1200His)	DOCK2 (R1200H)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 636506	NM_004946.3(DOCK2):c.4162A>T (p.Met1388Leu)	DOCK2 (M1388L)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 567059	NM_004946.3(DOCK2):c.5129C>T (p.Ala1710Val)	DOCK2 (A1710V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

ClinVar