ClinVar Miner

Submissions for variant NM_001655.5(ARCN1):c.4-60T>C

dbSNP: rs11216911
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001667586 SCV001890119 benign not provided 2021-05-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260292 SCV002539411 benign Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001667586 SCV005234616 benign not provided criteria provided, single submitter not provided

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