"Fulgent Genetics, Fulgent Genetics"[submitter] AND "ITGA8"[gene] - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779107	NM_003638.3(ITGA8):c.2977A>G (p.Ile993Val)	ITGA8 (I978V +1 more)	Single nucleotide variant (missense variant)	Renal hypodysplasia/aplasia 1 +1 more	GBenign/Likely benign
Select item 781192	NM_003638.3(ITGA8):c.2803G>A (p.Ala935Thr)	ITGA8 (A935T +1 more)	Single nucleotide variant (missense variant)	Renal hypodysplasia/aplasia 1 +1 more	GBenign/Likely benign
Select item 1601627	NM_003638.3(ITGA8):c.1400-11G>A	ITGA8	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign

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