List of variants in gene IFNGR2 reported as benign for autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_005534.4(IFNGR2):c.561+11C>G	rs11910627	0.77154
NM_005534.4(IFNGR2):c.191A>G (p.Gln64Arg)	rs9808753	0.17239
NM_005534.4(IFNGR2):c.173C>G (p.Thr58Arg)	rs4986958	0.04587
NM_005534.4(IFNGR2):c.721+7T>C	rs41351148	0.01141
NM_005534.4(IFNGR2):c.544A>G (p.Lys182Glu)	rs17878711	0.01107
NM_005534.4(IFNGR2):c.466A>C (p.Ile156Leu)	rs121913208	0.00206
NM_005534.4(IFNGR2):c.439G>A (p.Glu147Lys)	rs17878639	0.00115
NM_005534.4(IFNGR2):c.73+16G>A	rs571968917	0.00112
NM_005534.4(IFNGR2):c.231C>T (p.Ala77=)	rs150137842	0.00029
NM_005534.4(IFNGR2):c.234C>T (p.Asp78=)	rs138717312	0.00010
NM_005534.4(IFNGR2):c.74-6dup

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