Related gene-specific medical variations for Gene (Select 140894) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3158225	NM_033630.3(SCAND1):c.-78C>T	CNBD2, LOC130065772 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3158224	NM_033630.3(SCAND1):c.-78C>G	CNBD2, LOC130065772 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2341542	NM_033630.2(SCAND1):c.20G>A (p.Arg7Lys)	CNBD2, LOC130065773 +1 more (R7K)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2278039	NM_033630.2(SCAND1):c.46A>G (p.Ser16Gly)	CNBD2, SCAND1 (S16G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

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