"Centogene AG - the Rare Disease Company"[submitter] AND "COMP"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 988351	NM_000095.3(COMP):c.1153G>A (p.Asp385Asn)	COMP (D385N)	Single nucleotide variant (missense variant)	Carpal tunnel syndrome 2 +3 more	GPathogenic/Likely pathogenic
Select item 1333791	NM_000095.3(COMP):c.314C>T (p.Thr105Met)	COMP (T105M)	Single nucleotide variant (missense variant)	Multiple epiphyseal dysplasia type 1	GUncertain significance