ClinVar Miner

Submissions for variant NC_000011.9:g.105126944_105347752del220809

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
Medical Cytogenetics and Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano RCV000754455 SCV000787716 likely benign Primary amenorrhea 2018-06-01 criteria provided, single submitter research

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