ClinVar Miner

Submissions for variant NM_000158.3(GBE1):c.-195G>T

dbSNP: rs886058904
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 RCV000317541 SCV000446327 uncertain significance Glycogen storage disease, type IV 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000356130 SCV000446328 uncertain significance Adult polyglucosan body disease 2016-06-14 criteria provided, single submitter clinical testing

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