List of variants in gene BLNK reported as likely pathogenic for Agammaglobulinemia 4, 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_013314.4(BLNK):c.113+2T>G	rs2134092983
NM_013314.4(BLNK):c.145C>T (p.Arg49Ter)
NM_013314.4(BLNK):c.746+1G>A	rs2083906060
NM_013314.4(BLNK):c.747-2A>G

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