ClinVar Miner

Submissions for variant NM_001497.4(B4GALT1):c.412+44dup

dbSNP: rs111399879
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
Eurofins Ntd Llc (ga) RCV000596027 SCV000700478 uncertain significance not provided 2017-02-01 criteria provided, single submitter clinical testing
GeneDx RCV000596027 SCV001945393 benign not provided 2019-11-23 criteria provided, single submitter clinical testing

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