ClinVar Miner

List of variants in gene ALDH7A1 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_001182.5(ALDH7A1):c.1376T>C (p.Ile459Thr) rs1057518529
NM_001182.5(ALDH7A1):c.1489+4C>T rs775065938
NM_001182.5(ALDH7A1):c.201G>T (p.Thr67=) rs747643987
NM_001182.5(ALDH7A1):c.31_33delinsGAG (p.His11Glu) rs796052269
NM_001182.5(ALDH7A1):c.328C>G (p.Arg110Gly) rs121912708
NM_001182.5(ALDH7A1):c.364C>T (p.Arg122Trp) rs370624118
NM_001182.5(ALDH7A1):c.998C>T (p.Ala333Val) rs144625212

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.