ClinVar Miner

Submissions for variant NM_007289.4(MME):c.294C>T (p.Pro98=)

gnomAD frequency: 0.00003  dbSNP: rs200713056
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000929325 SCV001074954 likely benign not provided 2024-05-21 criteria provided, single submitter clinical testing

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