ClinVar Miner

Submissions for variant NM_000368.4(TSC1):c.*1785A>G (rs74362385)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000400966 SCV000478079 likely benign Tuberous sclerosis syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000314925 SCV000478080 likely benign Focal cortical dysplasia type II 2016-06-14 criteria provided, single submitter clinical testing

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