ClinVar Miner

Submissions for variant NM_002185.5(IL7R):c.800+10T>G

dbSNP: rs202114203
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001474192 SCV001678360 likely benign Immunodeficiency 104 2023-07-17 criteria provided, single submitter clinical testing

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