List of variants in gene IGLL1 reported as pathogenic for Agammaglobulinemia 2, autosomal recessive

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020070.4(IGLL1):c.425C>T (p.Pro142Leu)	rs1064422	0.00104
NM_020070.4(IGLL1):c.64C>T (p.Gln22Ter)	rs74315491	0.00001
NM_020070.4(IGLL1):c.258del (p.Gln88fs)	rs532338576

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