ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3234-130T>C

dbSNP: rs2725364
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252196 SCV000305352 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001618393 SCV001845532 benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002244070 SCV002514990 benign Werner syndrome 2021-12-05 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316350 SCV004016239 benign Wiskott-Aldrich syndrome 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001618393 SCV005264784 benign not provided criteria provided, single submitter not provided

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