ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.3087C>T (p.Cys1029=)

gnomAD frequency: 0.00015  dbSNP: rs141344823
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000714194 SCV000729282 likely benign not provided 2020-05-11 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000714194 SCV000844881 likely benign not provided 2018-05-01 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000714194 SCV000859073 uncertain significance not provided 2018-01-12 criteria provided, single submitter clinical testing
Invitae RCV000714194 SCV001051594 likely benign not provided 2024-01-08 criteria provided, single submitter clinical testing

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