ClinVar Miner

Submissions for variant NR_131224.1(H19):n.249+613T>A

dbSNP: rs431825169
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
UMR_S938_Pr. Le Bouc INSERM RCV000128485 SCV000114952 not provided Beckwith-Wiedemann syndrome no assertion provided not provided

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