ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1437C>T (p.Ala479=) (rs576806356)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001086920 SCV000166604 benign Multiple endocrine neoplasia, type 2 2019-12-31 criteria provided, single submitter clinical testing
Counsyl RCV000409774 SCV000489761 likely benign Multiple endocrine neoplasia, type 2b 2015-12-09 criteria provided, single submitter clinical testing
Counsyl RCV000410836 SCV000489762 likely benign Multiple endocrine neoplasia, type 2a 2015-12-09 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679714 SCV000807001 likely benign not provided 2017-05-05 criteria provided, single submitter clinical testing
Ambry Genetics RCV001011572 SCV001171909 likely benign Hereditary cancer-predisposing syndrome 2015-01-16 criteria provided, single submitter clinical testing

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