ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.*3848A>G (rs114213384)

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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 RCV000317228 SCV000403568 benign MAPT-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services,Illumina RCV000381503 SCV000483626 benign Syndromic intellectual disability 2016-06-14 criteria provided, single submitter clinical testing

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