ClinVar Miner

Submissions for variant NM_000381.4(MID1):c.1767T>C (p.Asn589=)

dbSNP: rs750022332
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) RCV000173681 SCV000224821 uncertain significance not provided 2016-03-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000173681 SCV004525050 benign not provided 2024-01-03 criteria provided, single submitter clinical testing

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