ClinVar Miner

Submissions for variant NM_005682.7(ADGRG1):c.26C>T (p.Thr9Met) (rs200241873)

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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 RCV000711842 SCV000842247 uncertain significance not provided 2018-03-27 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000765300 SCV000896555 uncertain significance Polymicrogyria, bilateral frontoparietal; Polymicrogyria, bilateral perisylvian, autosomal recessive 2018-10-31 criteria provided, single submitter clinical testing
Invitae RCV000711842 SCV001079360 likely benign not provided 2019-03-04 criteria provided, single submitter clinical testing

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