ClinVar Miner

Submissions for variant NM_001177316.2(SLC34A3):c.837G>A (p.Thr279=)

dbSNP: rs368153798
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000180375 SCV000232790 uncertain significance not provided 2015-04-27 criteria provided, single submitter clinical testing
GeneDx RCV000180375 SCV001811300 likely benign not provided 2020-12-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000180375 SCV003296629 likely benign not provided 2023-12-15 criteria provided, single submitter clinical testing

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