ClinVar Miner

Submissions for variant NM_002890.3(RASA1):c.-128GTT[2]

dbSNP: rs371042291
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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 RCV000366343 SCV000458937 likely benign Capillary malformation-arteriovenous malformation 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000269463 SCV000458938 likely benign Parkes Weber syndrome 2016-06-14 criteria provided, single submitter clinical testing

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