ClinVar Miner

Submissions for variant NM_170606.3(KMT2C):c.1299+15T>G

gnomAD frequency: 0.00022  dbSNP: rs180949226
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002139138 SCV002463194 benign not provided 2023-09-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002139138 SCV004157093 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing KMT2C: BS2

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