List of variants in gene ARSA reported as benign by Natera, Inc.

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000487.6(ARSA):c.1108-32C>T	rs762673	0.74934
NM_000487.6(ARSA):c.1178C>G (p.Thr393Ser)	rs743616	0.48362
NM_000487.6(ARSA):c.1055A>G (p.Asn352Ser)	rs2071421	0.19530
NM_000487.6(ARSA):c.459C>T (p.His153=)	rs6151412	0.05937
NM_000487.6(ARSA):c.1108-60C>T	rs873697	0.05763
NM_000487.6(ARSA):c.585G>T (p.Trp195Cys)	rs6151415	0.05295
NM_000487.6(ARSA):c.1493G>A (p.Arg498His)	rs6151428	0.04709
NM_000487.6(ARSA):c.1149C>T (p.Asp383=)	rs6151425	0.04013
NM_000487.6(ARSA):c.243C>T (p.Gly81=)	rs6151410	0.02425
NM_000487.6(ARSA):c.624T>C (p.His208=)	rs113990230	0.01000
NM_000487.6(ARSA):c.1002C>T (p.Ser334=)	rs147027229	0.00358
NM_000487.6(ARSA):c.659C>T (p.Pro220Leu)	rs201251634	0.00261
NM_000487.6(ARSA):c.1447G>A (p.Glu483Lys)	rs148352371	0.00245
NM_000487.6(ARSA):c.982G>A (p.Val328Met)	rs143994992	0.00022
NM_000487.6(ARSA):c.495G>A (p.Pro165=)	rs145299072
NM_000487.6(ARSA):c.530G>A (p.Gly177Asp)	rs556812341

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.