Related gene-specific medical variations for Gene (Select 3491) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139773	NM_001554.5(CCN1):c.76T>G (p.Cys26Gly)	CCN1, LOC129930877 (C26G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139769	NM_001554.5(CCN1):c.163G>T (p.Val55Phe)	CCN1, LOC129930878 (V55F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618958	NM_001554.5(CCN1):c.107C>T (p.Ala36Val)	CCN1, LOC129930877 (A36V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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