ClinVar Miner

Submissions for variant NM_001001557.4(GDF6):c.*271_*272insCTC

dbSNP: rs1554571161
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001545653 SCV001765029 likely benign not provided 2019-04-09 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000260930 SCV000475526 uncertain significance Klippel-Feil syndrome 2016-06-14 criteria provided, single submitter clinical testing

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