ClinVar Miner

Submissions for variant NM_198060.4(NRAP):c.994-13dup

dbSNP: rs35741231
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
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001700674 SCV001926304 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727978 SCV001975577 benign not specified no assertion criteria provided clinical testing

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