List of variants reported as likely pathogenic for immunodeficiency, common variable, 1

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.542C>A (p.Ala181Glu)	rs72553883	0.00518
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_012452.3(TNFRSF13B):c.260T>A (p.Ile87Asn)	rs72553877	0.00034
NM_012452.3(TNFRSF13B):c.204dup (p.Leu69fs)	rs72553875	0.00031
NM_012452.3(TNFRSF13B):c.61+2T>A	rs760885614	0.00001
NM_003998.4(NFKB1):c.1753-1G>C
NM_003998.4(NFKB1):c.850C>T (p.Arg284Ter)	rs1578793312
NM_005214.5(CTLA4):c.231_297delinsA (p.Gln80_Ser101del)
NM_012092.4(ICOS):c.136_139del (p.Asp46fs)
NM_012092.4(ICOS):c.394+2T>C	rs1559035937
NM_012092.4(ICOS):c.58+1G>A	rs757598952

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