ClinVar Miner

Submissions for variant NM_001001557.4(GDF6):c.*273CT[20]

dbSNP: rs71275339
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004696095 SCV005196032 uncertain significance not provided criteria provided, single submitter not provided
Illumina Laboratory Services, Illumina RCV000362793 SCV000475519 uncertain significance Klippel-Feil syndrome 2016-06-14 criteria provided, single submitter clinical testing

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