List of variants reported as likely benign for Immunodeficiency 27A

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005535.3(IL12RB1):c.641A>G (p.Gln214Arg)	rs11575934	0.25155
NM_005535.3(IL12RB1):c.467G>A (p.Arg156His)	rs11575926	0.11978
NM_000416.3(IFNGR1):c.*71G>T	rs55665036	0.00832
NM_000416.3(IFNGR1):c.489C>T (p.Pro163=)	rs41288981	0.00668
NM_005535.3(IL12RB1):c.783+10C>T	rs79972275	0.00554
NM_005535.3(IL12RB1):c.1719C>T (p.Ala573=)	rs17885102	0.00316
NM_000416.3(IFNGR1):c.181G>A (p.Val61Ile)	rs17175322	0.00253
NM_000416.3(IFNGR1):c.*128G>T	rs7769141	0.00213
NM_005534.4(IFNGR2):c.466A>C (p.Ile156Leu)	rs121913208	0.00206
NM_000416.3(IFNGR1):c.*462A>C	rs7750706	0.00202
NM_000416.3(IFNGR1):c.200+15T>G	rs17175329	0.00143
NM_000416.3(IFNGR1):c.1101G>A (p.Pro367=)	rs149761943	0.00122
NM_005534.4(IFNGR2):c.595T>C (p.Leu199=)	rs149173957	0.00043

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