C1838280[trait identifier] AND "Bioscientia Institut fuer Medizinische - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 635466	NM_000095.3(COMP):c.2150T>G (p.Met717Arg)	COMP (M717R)	Single nucleotide variant (missense variant)	Multiple epiphyseal dysplasia type 1	GUncertain significance
Select item 992397	NM_000095.3(COMP):c.1454G>A (p.Arg485His)	COMP (R485H)	Single nucleotide variant (missense variant)	Multiple epiphyseal dysplasia type 1	GUncertain significance