C4284592[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789266	NM_020738.4(KIDINS220):c.3586-7T>C	KIDINS220	Single nucleotide variant	not specified +3 more	GBenign/Likely benign
Select item 741480	NM_020738.4(KIDINS220):c.3318C>T (p.Ser1106=)	KIDINS220	Single nucleotide variant (synonymous variant +1 more)	Ventriculomegaly and arthrogryposis +2 more	GBenign/Likely benign
Select item 767781	NM_020738.4(KIDINS220):c.2568C>T (p.Leu856=)	KIDINS220	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 1619489	NM_020738.4(KIDINS220):c.2556A>G (p.Ala852=)	KIDINS220	Single nucleotide variant (synonymous variant +1 more)	Ventriculomegaly and arthrogryposis +2 more	GBenign/Likely benign

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