ClinVar Miner

Submissions for variant NM_002185.5(IL7R):c.83-18A>G

dbSNP: rs193922646
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000030066 SCV000052721 uncertain Severe combined immunodeficiency disease 2011-08-18 criteria provided, single submitter curation Converted during submission to Uncertain significance.

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