ClinVar Miner

List of variants in gene IFNGR2 reported as not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_005534.4(IFNGR2):c.74-3672C>T rs121913193 0.00964
NM_005534.4(IFNGR2):c.207-80G>A rs121913199 0.00263
NM_005534.4(IFNGR2):c.708A>T (p.Glu236Asp) rs121913212 0.00235
NM_005534.4(IFNGR2):c.466A>C (p.Ile156Leu) rs121913208 0.00206
NM_005534.4(IFNGR2):c.413-59A>G rs121913205 0.00036
NM_005534.4(IFNGR2):c.207-636C>T rs121913194 0.00029
NM_005534.4(IFNGR2):c.562-93C>T rs121913211 0.00027
NM_005534.4(IFNGR2):c.413-92T>C rs121913203 0.00007
NM_005534.4(IFNGR2):c.74-3937C>T rs121913192 0.00006
NM_005534.4(IFNGR2):c.207-123G>T rs121913197 0.00005
NM_005534.4(IFNGR2):c.207-109A>G rs121913198 0.00004
NM_005534.4(IFNGR2):c.413-197T>C rs121913202 0.00003
NM_005534.4(IFNGR2):c.510G>A (p.Thr170=) rs121913209 0.00003
NM_005534.4(IFNGR2):c.413-25T>C rs121913207 0.00001
NM_005534.4(IFNGR2):c.528T>C (p.Tyr176=) rs121913210 0.00001
NM_005534.4(IFNGR2):c.721+89T>C rs121913213 0.00001
NM_005534.4(IFNGR2):c.207-223A>G rs121913196
NM_005534.4(IFNGR2):c.207-407_207-406insATT rs121913195
NM_005534.4(IFNGR2):c.337C>T (p.Leu113=) rs121913200
NM_005534.4(IFNGR2):c.413-310A>C rs121913201
NM_005534.4(IFNGR2):c.413-53_413-48del rs137854906
NM_005534.4(IFNGR2):c.413-89AT[6] rs121913204

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