ClinVar Miner

Submissions for variant NM_003038.5(SLC1A4):c.40G>A (p.Ala14Thr)

gnomAD frequency: 0.00648  dbSNP: rs149636167
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
CeGaT Center for Human Genetics Tuebingen RCV000512758 SCV000608941 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing LINC02245: BS2; SLC1A4: PP2, BS2
Labcorp Genetics (formerly Invitae), Labcorp RCV000512758 SCV002371883 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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.