List of variants in gene combination IFNGR2, LOC119266102 reported as likely 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: 15

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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.39C>T (p.Leu13=)
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+10del
NM_005534.4(IFNGR2):c.73+7C>T
NM_005534.4(IFNGR2):c.73+8G>A	rs767210895
NM_005534.4(IFNGR2):c.73+9G>A
NM_005534.4(IFNGR2):c.73+9G>C
NM_005534.4(IFNGR2):c.9G>A (p.Pro3=)	rs762420616

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