List of variants in gene combination LRBA, MAB21L2 reported as pathogenic for Combined immunodeficiency due to LRBA deficiency

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
GRCh37/hg19 4q31.3(chr4:151441408-151719830)
NC_000004.11:g.(?_151336570)_(151520303_?)del
NC_000004.11:g.(?_151504182)_(151656538_?)del
NC_000004.12:g.(?_150415418)_(150817277_?)del

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