ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.1577-17T>G

gnomAD frequency: 0.00363  dbSNP: rs145080962
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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 RCV000246373 SCV000305345 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001589243 SCV001822443 likely benign not provided 2019-07-29 criteria provided, single submitter clinical testing
Invitae RCV002057395 SCV002489325 benign Werner syndrome 2024-01-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002057395 SCV002514971 benign Werner syndrome 2021-12-05 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316349 SCV004016248 benign Wiskott-Aldrich syndrome 2023-07-07 criteria provided, single submitter clinical testing

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