ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.3718T>G (p.Leu1240Val)

dbSNP: rs863225282
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000201906 SCV000256820 likely pathogenic Neuroblastoma, susceptibility to, 3 2015-11-03 no assertion criteria provided clinical testing

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