ClinVar Miner

Submissions for variant NM_001130823.3(DNMT1):c.2010C>T (p.Gly670=)

gnomAD frequency: 0.00027  dbSNP: rs374476495
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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
GeneDx RCV001704467 SCV000530629 likely benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Invitae RCV000876892 SCV001019527 benign Hereditary sensory neuropathy-deafness-dementia syndrome 2023-12-18 criteria provided, single submitter clinical testing

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