List of variants in gene combination IFNGR2, TMEM50B reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.984G>A (p.Lys328=)	rs121913220	0.00141
NM_005534.4(IFNGR2):c.722-91A>T	rs121913215	0.00112
NM_005534.4(IFNGR2):c.722-42C>T	rs121913216	0.00093
NM_005534.4(IFNGR2):c.721+173A>C	rs121913214	0.00028
NM_005534.4(IFNGR2):c.889G>A (p.Asp297Asn)	rs121913219	0.00007
NM_005534.4(IFNGR2):c.*352C>T	rs121913222	0.00003
NM_005534.4(IFNGR2):c.1008G>A (p.Thr336=)	rs121913221	0.00003
NM_005534.4(IFNGR2):c.780G>T (p.Ser260=)	rs121913217
NM_005534.4(IFNGR2):c.880-135_880-113dup	rs121913218

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