Related gene-specific medical variations for Gene (Select 6484) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 257675	NM_001254757.2(ST3GAL4):c.439T>C (p.Leu147=)	ST3GAL4	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign
Select item 257674	NM_001254757.2(ST3GAL4):c.423C>T (p.Tyr141=)	ST3GAL4	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign
Select item 257673	NM_001254757.2(ST3GAL4):c.252C>T (p.Tyr84=)	ST3GAL4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign

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