ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.-18+124C>G

gnomAD frequency: 0.12381  dbSNP: rs3744456
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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 RCV001518458 SCV001727153 benign Frontotemporal dementia 2025-01-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710286 SCV005246974 benign not provided criteria provided, single submitter not provided

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