ClinVar Miner

Submissions for variant NM_000616.5(CD4):c.1157-1G>A

dbSNP: rs782212142
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV001353064 SCV001548190 pathogenic Immunodeficiency 79 2021-03-25 no assertion criteria provided literature only

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