"ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 355063	NM_198239.2(CCN6):c.237C>T (p.Ala79=)	CCN6	Single nucleotide variant (synonymous variant +1 more)	Progressive pseudorheumatoid dysplasia +2 more	GBenign
Select item 500275	NM_198239.2(CCN6):c.533A>T (p.Asn178Ile)	CCN6 (N178I)	Single nucleotide variant (missense variant +1 more)	Progressive pseudorheumatoid dysplasia +3 more	GBenign/Likely benign