ClinVar Miner

Submissions for variant NM_001177316.2(SLC34A3):c.1473C>T (p.Tyr491=)

gnomAD frequency: 0.00022  dbSNP: rs148095831
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000594295 SCV000701960 uncertain significance not provided 2016-10-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000594295 SCV001727593 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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