ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 reported as pathogenic for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP
NC_000009.11:g.(?_119460002)_(119462003_?)del
NM_012210.3(TRIM32):c.1108del (p.Met370fs) rs759376012
NM_012210.3(TRIM32):c.1459G>A (p.Asp487Asn) rs111033570
NM_012210.3(TRIM32):c.388C>T (p.Pro130Ser) rs111033571

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.