ClinVar Miner

Submissions for variant NM_002074.5(GNB1):c.267+7A>G

dbSNP: rs1646696544
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001334996 SCV001528019 uncertain significance Intellectual disability, autosomal dominant 42 2018-03-12 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Labcorp Genetics (formerly Invitae), Labcorp RCV002070196 SCV002337573 likely benign not provided 2023-10-12 criteria provided, single submitter clinical testing

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