ClinVar Miner

List of variants in gene combination KIRREL2, NPHS1 reported as uncertain significance for Finnish congenital nephrotic syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_004646.3(NPHS1):c.-31C>T rs376050812
NM_004646.3(NPHS1):c.-475_-468delGAGAGAGA rs139954720
NM_004646.3(NPHS1):c.-57G>T rs140404523
NM_004646.3(NPHS1):c.-61G>A rs75799457
NM_004646.3(NPHS1):c.41T>C (p.Leu14Pro) rs1060499706
NM_004646.3(NPHS1):c.65C>T (p.Ala22Val) rs116617171

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.