"Baylor Genetics"[submitter] AND "SLC29A3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2441776	NM_018344.6(SLC29A3):c.2-4A>G	SLC29A3	Single nucleotide variant (intron variant)	H syndrome	GLikely pathogenic
Select item 576880	NM_018344.6(SLC29A3):c.707C>T (p.Thr236Met)	SLC29A3 (T236M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity