ClinVar Miner

Submissions for variant NM_007325.5(GRIA3):c.751-16T>C

gnomAD frequency: 0.58620  dbSNP: rs550640
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001703315 SCV001933957 benign Syndromic X-linked intellectual disability 94 2021-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002077169 SCV002409128 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002077169 SCV005278016 benign not provided criteria provided, single submitter not provided

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