ClinVar Miner

Submissions for variant NM_000206.3(IL2RG):c.758-1G>C

dbSNP: rs886042051
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
CeGaT Center for Human Genetics Tuebingen RCV001531160 SCV001746147 pathogenic not provided 2021-05-01 criteria provided, single submitter clinical testing

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