ClinVar Miner

Submissions for variant NM_017827.4(SARS2):c.696C>T (p.Arg232=)

gnomAD frequency: 0.00118  dbSNP: rs35389151
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000907774 SCV000520019 likely benign not provided 2020-12-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000907774 SCV001052500 benign not provided 2024-01-02 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002481305 SCV002803757 likely benign Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome 2021-09-15 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000907774 SCV002822562 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing SARS2: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000907774 SCV005208319 likely benign not provided criteria provided, single submitter not provided

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.