ClinVar Miner

List of variants reported as uncertain significance for Combined immunodeficiency, X-linked by Genome-Nilou Lab

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000206.3(IL2RG):c.1061A>G (p.His354Arg) rs771221019 0.00002
NM_000206.3(IL2RG):c.318A>G (p.Leu106=) rs1389116834

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