ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.1020G>A (p.Thr340=) (rs142539117)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000710544 SCV000840785 benign not provided 2017-09-01 criteria provided, single submitter clinical testing
Ambry Genetics RCV000715684 SCV000846515 benign Autism spectrum disorder 2016-03-13 criteria provided, single submitter clinical testing

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