ClinVar Miner

Submissions for variant NM_170606.3(KMT2C):c.10759C>G (p.Gln3587Glu)

gnomAD frequency: 0.00002  dbSNP: rs567451018
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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
Mendelics RCV002249263 SCV002518500 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003774712 SCV004696207 likely benign not provided 2023-04-04 criteria provided, single submitter clinical testing

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