Related gene-specific medical variations for Gene (Select 3177) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3164059	NM_001532.3(SLC29A2):c.1337C>A (p.Ala446Asp)	B4GAT1-DT, SLC29A2 (A446D)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3164058	NM_001532.3(SLC29A2):c.1291G>A (p.Gly431Ser)	B4GAT1-DT, SLC29A2 (G431S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance