ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.1296G>C (p.Thr432=) (rs74033734)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000517804 SCV000612329 benign not specified 2017-06-26 criteria provided, single submitter clinical testing
Ambry Genetics RCV000715968 SCV000846800 benign Autism spectrum disorder 2016-06-06 criteria provided, single submitter clinical testing
Invitae RCV000864300 SCV001005086 benign not provided 2019-02-14 criteria provided, single submitter clinical testing

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