ClinVar Miner

Submissions for variant NM_170606.3(KMT2C):c.7236C>T (p.Pro2412=)

dbSNP: rs140215243
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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 RCV002102691 SCV002389837 likely benign not provided 2023-11-27 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002499920 SCV002804817 likely benign Kleefstra syndrome 2 2021-12-30 criteria provided, single submitter clinical testing

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