List of variants in gene IDS reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000202.8(IDS):c.123C>G (p.Leu41=)	rs146904022	0.00115
NM_000202.8(IDS):c.126C>T (p.Ile42=)	rs146963087	0.00115
NM_000202.8(IDS):c.104A>G (p.Asp35Gly)	rs144081417	0.00020
NM_000202.8(IDS):c.1285G>A (p.Val429Ile)	rs781916566	0.00001
NM_000202.8(IDS):c.*1G>C	rs2089302571
NM_000202.8(IDS):c.103+4C>T
NM_000202.8(IDS):c.1608T>C (p.Tyr536=)	rs2089303285
NM_000202.8(IDS):c.353C>T (p.Thr118Ile)	rs2520895871
NM_000202.8(IDS):c.400G>A (p.Gly134Arg)	rs2520895308

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.