ClinVar Miner

Submissions for variant NM_144969.3(ZDHHC15):c.747C>T (p.Cys249=)

gnomAD frequency: 0.00049  dbSNP: rs147278537
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
Eurofins Ntd Llc (ga) RCV000180703 SCV000233183 benign not specified 2015-01-06 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000180703 SCV002066135 benign not specified 2019-08-05 criteria provided, single submitter clinical testing

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