List of variants in gene combination IFNGR2, TMEM50B reported as benign for autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005534.4(IFNGR2):c.879+19C>T	rs17883129	0.37206
NM_005534.4(IFNGR2):c.978G>A (p.Pro326=)	rs17885407	0.00181
NM_005534.4(IFNGR2):c.984G>A (p.Lys328=)	rs121913220	0.00141
NM_005534.4(IFNGR2):c.879+19del	rs193922682	0.00070
NM_005534.4(IFNGR2):c.879+18dup	rs201322939
NM_005534.4(IFNGR2):c.879+19_879+20del	rs750203174
NM_005534.4(IFNGR2):c.879+31_879+32dup	rs143248516
NM_005534.4(IFNGR2):c.879+32del	rs143248516
NM_005534.4(IFNGR2):c.879+32dup	rs143248516

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