Related gene-specific medical variations for Gene (Select 57228) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3166260	NM_001031628.2(SMAGP):c.259G>T (p.Ala87Ser)	DAZAP2, SMAGP (A87S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601154	NM_001031628.2(SMAGP):c.218A>C (p.Glu73Ala)	DAZAP2, SMAGP (E73A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358883	NM_001031628.2(SMAGP):c.249G>C (p.Glu83Asp)	DAZAP2, SMAGP (E83D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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