ClinVar Miner

Submissions for variant NM_000514.4(GDNF):c.*131GGA[10]

dbSNP: rs150577324
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000362220 SCV000457480 likely benign Hirschsprung Disease, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001692017 SCV001913901 benign not provided 2021-06-19 criteria provided, single submitter clinical testing

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