List of variants in gene combination DYNC1H1, LOC126862060 reported as uncertain significance for Intellectual disability, autosomal dominant 13

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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.8929C>T (p.Arg2977Trp)	rs2503804194
NM_001376.5(DYNC1H1):c.9092C>T (p.Thr3031Met)	rs879253956
NM_001376.5(DYNC1H1):c.9286G>A (p.Asp3096Asn)	rs2503805793
NM_001376.5(DYNC1H1):c.9436A>G (p.Ser3146Gly)	rs2048470658

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.