ClinVar Miner

Submissions for variant NM_000404.4(GLB1):c.-35T>G

dbSNP: rs886058344
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000370265 SCV000443205 uncertain significance Morquio syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000273433 SCV000443206 uncertain significance GM1 gangliosidosis 2016-06-14 criteria provided, single submitter clinical testing

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