ClinVar Miner

Submissions for variant NM_001303052.2(MYT1L):c.3033A>T (p.Gly1011=)

dbSNP: rs6728368
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001671418 SCV001888638 benign not provided 2018-08-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502014 SCV002805300 likely benign Intellectual disability, autosomal dominant 39 2022-04-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001671418 SCV005283740 benign not provided criteria provided, single submitter not provided

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