ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.*2510_*2515del

dbSNP: rs549171175
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000277907 SCV000347375 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing

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