ClinVar Miner

Submissions for variant NM_007325.5(GRIA3):c.268+16762dup

dbSNP: rs11452643
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000990936 SCV001142006 benign Syndromic X-linked intellectual disability 94 2019-05-28 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000990936 SCV004562774 benign Syndromic X-linked intellectual disability 94 2024-11-22 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699498 SCV001927071 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001726409 SCV001963706 likely benign not provided no assertion criteria provided clinical testing

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