ClinVar Miner

Submissions for variant NM_012259.3(HEY2):c.328+32del

dbSNP: rs2243357
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
Clinical Genetics, Academic Medical Center RCV001795493 SCV002034381 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001795493 SCV002035174 benign not specified no assertion criteria provided clinical testing

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