ClinVar Miner

Submissions for variant NM_000368.5(TSC1):c.-174A>T

dbSNP: rs886063627
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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 RCV000291514 SCV000478280 uncertain significance Isolated focal cortical dysplasia type II 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000346388 SCV000478281 uncertain significance Tuberous sclerosis syndrome 2016-06-14 criteria provided, single submitter clinical testing

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