C1970431[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 139413	NM_001083962.2(TCF4):c.*5-10C>T	TCF4	Single nucleotide variant (intron variant)	Pitt-Hopkins syndrome +2 more	GBenign/Likely benign
Select item 468954	NM_001083962.2(TCF4):c.1990G>T (p.Ala664Ser)	TCF4 (A664S +21 more)	Single nucleotide variant (missense variant)	Corneal dystrophy, Fuchs endothelial, 3 +1 more	GUncertain significance
Select item 381239	NM_001083962.2(TCF4):c.923-17G>T	TCF4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign

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