C1853392[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 878604	NM_000417.3(IL2RA):c.655+4C>T	IL2RA	Single nucleotide variant (intron variant)	Type 1 diabetes mellitus 10 +2 more	GUncertain significance
Select item 950359	NM_000417.3(IL2RA):c.499G>A (p.Val167Ile)	IL2RA (V167I)	Single nucleotide variant (missense variant +1 more)	Type 1 diabetes mellitus 10 +1 more	GUncertain significance
Select item 1021454	NM_000417.3(IL2RA):c.125A>G (p.Lys42Arg)	IL2RA (K42R)	Single nucleotide variant (missense variant)	Type 1 diabetes mellitus 10 +1 more	GUncertain significance

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