ClinVar Miner

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

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_005534.4(IFNGR2):c.9G>C (p.Pro3=) rs762420616 0.00003
NM_005534.4(IFNGR2):c.51C>T (p.Ala17=) rs1450348387 0.00002
NM_005534.4(IFNGR2):c.73+10G>T rs990250212 0.00002
NM_005534.4(IFNGR2):c.73+8G>T rs767210895 0.00001
NM_005534.4(IFNGR2):c.13C>T (p.Leu5=)
NM_005534.4(IFNGR2):c.16C>T (p.Leu6=) rs2123322462
NM_005534.4(IFNGR2):c.45C>G (p.Val15=) rs2123322539
NM_005534.4(IFNGR2):c.48C>T (p.Phe16=)
NM_005534.4(IFNGR2):c.73+8G>A rs767210895
NM_005534.4(IFNGR2):c.9G>A (p.Pro3=) rs762420616

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