ClinVar Miner

Submissions for variant NM_002010.3(FGF9):c.*274_*277del

dbSNP: rs201279299
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000388210 SCV000383193 uncertain significance Symphalangism-brachydactyly syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693141 SCV005192081 uncertain significance not provided criteria provided, single submitter not provided

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