ClinVar Miner

List of variants in gene combination IFNGR2, LOC119266102 reported as pathogenic for Immunodeficiency 28

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_005534.4(IFNGR2):c.1A>G (p.Met1Val) rs1316638883 0.00001
NM_005534.4(IFNGR2):c.4del (p.Arg2fs) rs2083655919

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