ClinVar Miner

Submissions for variant NM_000381.4(MID1):c.1663A>C (p.Ile555Leu)

gnomAD frequency: 0.00005  dbSNP: rs398123341
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) RCV000078677 SCV000110537 uncertain significance not provided 2013-11-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000078677 SCV004633901 benign not provided 2024-02-20 criteria provided, single submitter clinical testing

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