List of variants in gene SLC29A3 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018344.6(SLC29A3):c.946T>G (p.Phe316Val)	rs139066012	0.00076
NM_018344.6(SLC29A3):c.269C>T (p.Thr90Ile)	rs138389471	0.00013
NM_018344.6(SLC29A3):c.1124A>G (p.Asn375Ser)	rs150398575	0.00006

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