ClinVar Miner

Submissions for variant NM_172341.4(PSENEN):c.61+17G>C (rs10402601)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000605712 SCV000745376 benign Acne inversa, familial, 2 2015-09-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000605712 SCV000733873 benign Acne inversa, familial, 2 no assertion criteria provided clinical testing
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam RCV000605712 SCV000745894 benign Acne inversa, familial, 2 2016-01-15 no assertion criteria provided clinical testing

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