ClinVar Miner

Submissions for variant NM_181303.2(NLGN3):c.707A>G (p.Asn236Ser)

dbSNP: rs2092405042
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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 RCV001329099 SCV001520427 uncertain significance Autism, susceptibility to, X-linked 1 2019-11-05 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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