ClinVar Miner

Submissions for variant NM_000123.3(ERCC5):c.2879+14C>T (rs4150360)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000606280 SCV000745534 benign Xeroderma pigmentosum, group G 2015-09-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000606280 SCV000733198 benign Xeroderma pigmentosum, group G no assertion criteria provided clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000297213 SCV000382121 benign Xeroderma pigmentosum 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000251774 SCV000302361 benign not specified criteria provided, single submitter clinical testing

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