ClinVar Miner

Submissions for variant NM_025103.4(IFT74):c.1624-1G>A

dbSNP: rs2489749390
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA-diagnostics Laboratory, Research Centre For Medical Genetics RCV004578006 SCV005061821 uncertain significance Bardet-Biedl syndrome 22 criteria provided, single submitter clinical testing

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