ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1707+109G>T

dbSNP: rs78601535
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
GeneDx RCV001592331 SCV001823886 likely benign not provided 2018-08-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001592331 SCV005225342 likely benign not provided criteria provided, single submitter not provided

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