C1845366[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333886	NM_002547.3(OPHN1):c.1226G>A (p.Arg409His)	OPHN1 (R409H)	Single nucleotide variant (missense variant)	X-linked intellectual disability-cerebellar hypoplasia syndrome +1 more	GUncertain significance
Select item 1333887	NM_002547.3(OPHN1):c.812A>G (p.Tyr271Cys)	OPHN1 (Y271C)	Single nucleotide variant (missense variant)	X-linked intellectual disability-cerebellar hypoplasia syndrome	GUncertain significance