ClinVar Miner

Submissions for variant NM_007325.5(GRIA3):c.268+16792G>A

dbSNP: rs1927781157
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001333569 SCV001526192 uncertain significance Syndromic X-linked intellectual disability 94 2018-04-11 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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