C1858723[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1013673	NM_024598.4(USB1):c.209G>A (p.Arg70Gln)	USB1 (R19Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1028327	NM_024598.4(USB1):c.253G>A (p.Val85Ile)	USB1 (V34I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1032181	NM_024598.4(USB1):c.796T>G (p.Ter266Gly)	USB1	Single nucleotide variant (stop lost)	Poikiloderma with neutropenia	GUncertain significance

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