ClinVar Miner

List of variants in gene CA2 reported as uncertain significance 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: 10
Download table as spreadsheet
NM_000067.3(CA2):c.*17G>A rs140653628
NM_000067.3(CA2):c.*303C>T rs150089617
NM_000067.3(CA2):c.*374A>G rs886063151
NM_000067.3(CA2):c.*465A>C rs886063152
NM_000067.3(CA2):c.*562T>C rs886063153
NM_000067.3(CA2):c.139_142CTGT[1] (p.Ser48fs) rs1564077060
NM_000067.3(CA2):c.40G>A (p.Glu14Lys) rs758659684
NM_000067.3(CA2):c.508-7G>A rs886063149
NM_000067.3(CA2):c.539C>T (p.Pro180Leu) rs886063150
NM_000067.3(CA2):c.648C>T (p.Ser216=) rs376387073

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.