ClinVar Miner

Submissions for variant NM_207361.6(FREM2):c.*5627del

dbSNP: rs5802961
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000385673 SCV000384335 benign Fraser syndrome 1 2016-06-14 criteria provided, single submitter clinical testing

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