List of variants in gene SLC29A3 reported as likely benign by Genetic Services Laboratory, University 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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018344.6(SLC29A3):c.383+8A>G	rs2243540	0.87580
NM_018344.6(SLC29A3):c.976A>G (p.Ile326Val)	rs2487068	0.87306
NM_018344.6(SLC29A3):c.714T>C (p.Thr238=)	rs2252997	0.86524
NM_018344.6(SLC29A3):c.715G>A (p.Val239Ile)	rs2252996	0.84172
NM_018344.6(SLC29A3):c.1008T>C (p.Gly336=)	rs1084004	0.83737
NM_018344.6(SLC29A3):c.473C>T (p.Ser158Phe)	rs780668	0.61038
NM_018344.6(SLC29A3):c.52A>G (p.Arg18Gly)	rs2277257	0.47837
NM_018344.6(SLC29A3):c.831C>T (p.Pro277=)	rs61737431	0.01828
NM_018344.6(SLC29A3):c.842T>C (p.Leu281Pro)	rs79737301	0.01805
NM_018344.6(SLC29A3):c.304T>C (p.Tyr102His)	rs77339410	0.01738

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.