List of variants reported as uncertain significance for syndromic intellectual disability by Provincial Medical Genetics Program of British Columbia, University of British Columbia

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

Total variants: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001032382.2(PQBP1):c.530G>A (p.Arg177His)	rs1047322213
NM_001376.5(DYNC1H1):c.9092C>T (p.Thr3031Met)	rs879253956
NM_007118.4(TRIO):c.3332-1_3332del	rs2152351137
NM_030665.4(RAI1):c.3660T>A (p.His1220Gln)	rs745379131

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.