ClinVar Miner

Submissions for variant NM_005909.5(MAP1B):c.5563G>C (p.Gly1855Arg)

dbSNP: rs2478583495
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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 RCV003148343 SCV003835111 uncertain significance Periventricular nodular heterotopia 9 2021-07-21 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148344 SCV003835144 uncertain significance Hearing loss, autosomal dominant 83 2021-07-21 criteria provided, single submitter clinical testing

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