ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.355+20A>T

gnomAD frequency: 0.04393  dbSNP: rs4987239
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247141 SCV000305354 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001618394 SCV001847579 benign not provided 2018-08-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057396 SCV002402836 benign Werner syndrome 2024-02-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002057396 SCV002514962 benign Werner syndrome 2021-12-05 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316351 SCV004016234 benign Wiskott-Aldrich syndrome 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001618394 SCV005271844 benign not provided criteria provided, single submitter not provided

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