ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.1464+20T>C

dbSNP: rs886038740
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243292 SCV000316364 likely benign not specified criteria provided, single submitter clinical testing
Counsyl RCV000671460 SCV000796436 likely benign Ellis-van Creveld syndrome 2017-12-14 criteria provided, single submitter clinical testing

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