ClinVar Miner

Submissions for variant NM_000514.4(GDNF):c.-227_-225CGG[6] (rs554953764)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000300387 SCV000484137 likely benign Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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