ClinVar Miner

Submissions for variant NM_172351.3(CD46):c.-6C>T

gnomAD frequency: 0.00004  dbSNP: rs886045836
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000388658 SCV000353475 uncertain significance Atypical hemolytic-uremic syndrome 2016-06-14 criteria provided, single submitter clinical testing

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