ClinVar Miner

Submissions for variant NM_002890.3(RASA1):c.2691-11C>T (rs149730288)

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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 RCV000337398 SCV000458991 likely benign Capillary malformation-arteriovenous malformation 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000396388 SCV000458992 likely benign Parkes Weber syndrome 2016-06-14 criteria provided, single submitter clinical testing

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