ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.1802G>T (p.Gly601Val)

gnomAD frequency: 0.00021  dbSNP: rs143613619
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000896115 SCV001040192 benign not provided 2024-11-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV002540143 SCV003707726 uncertain significance Inborn genetic diseases 2021-10-21 criteria provided, single submitter clinical testing The c.1727G>T (p.G576V) alteration is located in exon 15 (coding exon 15) of the DVL1 gene. This alteration results from a G to T substitution at nucleotide position 1727, causing the glycine (G) at amino acid position 576 to be replaced by a valine (V). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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.