ClinVar Miner

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

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_001365068.1(ASTN2):c.2806+24861A>G rs2281627
NM_001365068.1(ASTN2):c.2806+26703A>T rs1372713940
NM_001365068.1(ASTN2):c.2806+26775C>T rs1661300
NM_001365068.1(ASTN2):c.2806+26889G>A rs142715198
NM_001365068.1(ASTN2):c.2806+27369C>G rs3747833
NM_012210.3(TRIM32):c.-133G>C rs12342207

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.