C0272167[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 578484	NM_001625.4(AK2):c.631G>A (p.Asp211Asn)	AK2 (D211N +3 more)	Single nucleotide variant (missense variant +2 more)	Reticular dysgenesis	GUncertain significance
Select item 728081	NM_001625.4(AK2):c.615G>C (p.Gly205=)	AK2	Single nucleotide variant (synonymous variant +2 more)	AK2-related disorder +1 more	GLikely benign
Select item 577089	NM_001625.4(AK2):c.247A>G (p.Ile83Val)	AK2 (I83V +2 more)	Single nucleotide variant (missense variant +1 more)	Reticular dysgenesis	GUncertain significance

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