ClinVar Miner

Submissions for variant NM_007289.4(MME):c.1417-18A>G

gnomAD frequency: 0.00001  dbSNP: rs1219891459
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 RCV001945756 SCV002198478 likely benign not provided 2024-11-22 criteria provided, single submitter clinical testing

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