ClinVar Miner

List of variants in gene ALDH7A1 reported as uncertain significance for Seizures

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_001182.4(ALDH7A1):c.1493_1495delGAG (p.Gly498del) rs796052268
NM_001182.5(ALDH7A1):c.1073G>T (p.Arg358Leu) rs144671885
NM_001182.5(ALDH7A1):c.1232C>T (p.Pro411Leu) rs780233639
NM_001182.5(ALDH7A1):c.154G>C (p.Glu52Gln) rs765562932
NM_001182.5(ALDH7A1):c.364C>T (p.Arg122Trp) rs370624118
NM_001182.5(ALDH7A1):c.394-5T>C rs1299570489
NM_001182.5(ALDH7A1):c.452T>C (p.Val151Ala) rs1561667040
NM_001182.5(ALDH7A1):c.56C>T (p.Ser19Phe) rs566243475
NM_001182.5(ALDH7A1):c.623C>T (p.Ala208Val) rs200433565
NM_001182.5(ALDH7A1):c.651-5T>C rs770931075
NM_001182.5(ALDH7A1):c.995C>G (p.Thr332Ser) rs543182575

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.