ClinVar Miner

List of variants in gene IFNG reported as uncertain significance for anemia

Included ClinVar conditions (280):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_000619.3(IFNG):c.183+15C>G rs199708992 0.00081
NM_000619.3(IFNG):c.114+11C>T rs200610212 0.00070
NM_000619.3(IFNG):c.-5A>G rs181407537 0.00066
NM_000619.3(IFNG):c.285C>T (p.Thr95=) rs142375196 0.00009
NM_000619.3(IFNG):c.*231T>C rs1413472447 0.00001
NM_000619.3(IFNG):c.-34T>G rs752463155 0.00001
NM_000619.3(IFNG):c.431C>T (p.Ser144Leu) rs753611452 0.00001
NM_000619.3(IFNG):c.*107A>G rs886049800
NM_000619.3(IFNG):c.*187T>G rs1213374453
NM_000619.3(IFNG):c.*22T>A rs1882583669
NM_000619.3(IFNG):c.*93TCAA[1] rs137854903
NM_000619.3(IFNG):c.*9C>T rs886049801
NM_000619.3(IFNG):c.-2C>A rs886049802
NM_000619.3(IFNG):c.-9T>C rs886049803
NM_000619.3(IFNG):c.431C>A (p.Ser144Ter) rs753611452

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