ClinVar Miner

Submissions for variant NM_024597.4(MAP7D3):c.347G>A (p.Arg116Gln)

dbSNP: rs62640387
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000972142 SCV001119836 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000972142 SCV001150456 uncertain significance not provided 2016-10-01 criteria provided, single submitter clinical testing

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