ClinVar Miner

List of variants in gene APOA1 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_000039.2(APOA1):c.*19C>G rs187335584
NM_000039.2(APOA1):c.-11G>A rs199729971
NM_000039.2(APOA1):c.181G>A (p.Ala61Thr) rs12718465
NM_000039.2(APOA1):c.284T>A (p.Phe95Tyr) rs138407155
NM_000039.2(APOA1):c.454G>A (p.Glu152Lys) rs574061789
NM_000039.2(APOA1):c.732C>G (p.Pro244=) rs5080

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.