List of variants in gene IFNG studied for anemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000619.3(IFNG):c.*180C>T	rs2069722	0.01606
NM_000619.3(IFNG):c.*539A>G	rs2069723	0.01255
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.*500C>T	rs528060683	0.00016
NM_000619.3(IFNG):c.285C>T (p.Thr95=)	rs142375196	0.00009
NM_000619.3(IFNG):c.*465A>T	rs532081510	0.00004
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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