ClinVar Miner

Submissions for variant NM_000452.3(SLC10A2):c.39T>C (p.Val13=)

dbSNP: rs201994393
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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) RCV000596826 SCV000706293 uncertain significance not provided 2017-02-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000596826 SCV003013435 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing

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