ClinVar Miner

Submissions for variant NM_001324144.2(ZNF41):c.-280+483GCACGC[3]

dbSNP: rs200168272
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000403527 SCV000482430 uncertain significance Non-syndromic X-linked intellectual disability 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004696178 SCV005192407 uncertain significance not provided criteria provided, single submitter not provided

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