List of variants reported as benign for Agammaglobulinemia 4, autosomal recessive by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_013314.4(BLNK):c.1096-11A>T	rs74151283	0.05315
NM_013314.4(BLNK):c.48G>A (p.Arg16=)	rs11540858	0.03732
NM_013314.4(BLNK):c.195C>T (p.Ser65=)	rs12261820	0.01993
NM_013314.4(BLNK):c.526-5G>C	rs17111459	0.01232
NM_013314.4(BLNK):c.362-17T>C	rs118063042	0.00879
NM_013314.4(BLNK):c.472G>T (p.Ala158Ser)	rs148612299	0.00489
NM_013314.4(BLNK):c.270G>A (p.Glu90=)	rs17111469	0.00302
NM_013314.4(BLNK):c.262G>A (p.Ala88Thr)	rs144903484	0.00175
NM_013314.4(BLNK):c.132T>A (p.Pro44=)	rs147203646	0.00125
NM_013314.4(BLNK):c.1096-16A>T	rs80026049	0.00035
NM_013314.4(BLNK):c.744C>T (p.Ala248=)	rs147455437	0.00005
NM_013314.4(BLNK):c.164-9C>T	rs587723501	0.00001
NM_013314.4(BLNK):c.1096-17del	rs201454460
NM_013314.4(BLNK):c.1096-9dup
NM_013314.4(BLNK):c.171T>C (p.Pro57=)	rs727852
NM_013314.4(BLNK):c.48-5dup
NM_013314.4(BLNK):c.608-22CA[5]	rs200821324
NM_013314.4(BLNK):c.775-12del

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