ClinVar Miner

List of variants reported as uncertain significance for Alternating hemiplegia of childhood 1; Familial hemiplegic migraine type 2 by Fulgent Genetics,Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
NM_000702.4(ATP1A2):c.1097G>A (p.Gly366Asp)
NM_000702.4(ATP1A2):c.1282C>T (p.Arg428Cys) rs779985796
NM_000702.4(ATP1A2):c.1690C>T (p.Arg564Trp) rs762330744
NM_000702.4(ATP1A2):c.192G>T (p.Gln64His) rs796052282
NM_000702.4(ATP1A2):c.2062G>T (p.Ala688Ser)
NM_000702.4(ATP1A2):c.2675T>C (p.Met892Thr) rs794727222
NM_000702.4(ATP1A2):c.2680G>T (p.Asp894Tyr) rs1553245907
NM_000702.4(ATP1A2):c.2770G>A (p.Val924Met) rs373276446
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr) rs181618883

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.