ClinVar Miner

Submissions for variant NM_018238.4(AGK):c.*1233_*1236del

dbSNP: rs886062028
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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 RCV000268303 SCV000467079 uncertain significance Developmental cataract 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000321107 SCV000467080 uncertain significance Sengers syndrome 2016-06-14 criteria provided, single submitter clinical testing

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