ClinVar Miner

Submissions for variant NM_007325.5(GRIA3):c.268+16757dup

dbSNP: rs778944548
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000203157 SCV000257854 benign not specified 2015-05-05 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000608382 SCV000734738 benign Syndromic X-linked intellectual disability 94 no assertion criteria provided clinical testing

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