ClinVar Miner

Submissions for variant NM_001330078.2(NRXN1):c.549G>A (p.Trp183Ter)

dbSNP: rs1416806597
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV001806987 SCV002051680 uncertain significance not provided 2021-01-12 criteria provided, single submitter clinical testing PM2

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