List of variants in gene SLC39A7 reported as benign for not provided

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006979.3(SLC39A7):c.627C>G (p.Ser209=)	rs1547387	0.08405
NM_006979.3(SLC39A7):c.581-10C>A	rs41266701	0.07067
NM_006979.3(SLC39A7):c.370G>C (p.Gly124Arg)	rs35690712	0.02915
NM_006979.3(SLC39A7):c.259G>A (p.Asp87Asn)	rs34211188	0.02642
NM_006979.3(SLC39A7):c.471C>T (p.Pro157=)	rs11538810	0.00928
NM_006979.3(SLC39A7):c.160T>C (p.Phe54Leu)	rs76929655	0.00841
NM_006979.3(SLC39A7):c.744T>C (p.His248=)	rs113198103	0.00753
NM_006979.3(SLC39A7):c.171C>A (p.Gly57=)	rs2975297	0.00156
NM_006979.3(SLC39A7):c.847A>C (p.Thr283Pro)	rs200100279	0.00036
NM_006979.3(SLC39A7):c.789T>C (p.His263=)	rs34836401	0.00028
NM_006979.3(SLC39A7):c.1057A>G (p.Met353Val)	rs200791329	0.00020

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.