ClinVar Miner

List of variants reported as uncertain significance for aortic valve disease 3

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_019055.6(ROBO4):c.691T>A (p.Tyr231Asn) rs149517154 0.00027
NM_019055.6(ROBO4):c.190C>T (p.Arg64Cys) rs201393279 0.00019
NM_019055.6(ROBO4):c.1471C>T (p.Arg491Cys) rs374471211 0.00010
NM_019055.6(ROBO4):c.1678C>T (p.Arg560Cys)
NM_019055.6(ROBO4):c.184A>G (p.Thr62Ala)
NM_019055.6(ROBO4):c.1900C>T (p.Arg634Cys)
NM_019055.6(ROBO4):c.2182C>T (p.Gln728Ter)
NM_019055.6(ROBO4):c.2758G>A (p.Gly920Ser)
NM_019055.6(ROBO4):c.746T>C (p.Leu249Pro)

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.