ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.2395A>G (p.Arg799Gly)

dbSNP: rs1715095634
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004782693 SCV005394197 uncertain significance not specified 2024-09-27 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278321 SCV001465321 uncertain significance Ellis-van Creveld syndrome 2020-08-13 no assertion criteria provided clinical testing

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