ClinVar Miner

Submissions for variant NM_001282531.3(ADNP):c.2978C>G (p.Pro993Arg)

dbSNP: rs1251589256
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002246944 SCV002516844 uncertain significance not specified 2022-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003094046 SCV003304721 likely benign not provided 2024-02-19 criteria provided, single submitter clinical testing

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