List of variants in gene NFKB2 reported as likely pathogenic for B cell deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001322934.2(NFKB2):c.104-1G>C	rs2061116343
NM_001322934.2(NFKB2):c.1359_1363dup (p.Gln455fs)
NM_001322934.2(NFKB2):c.2576_2580del (p.Thr859fs)	rs1565214594
NM_001322934.2(NFKB2):c.2595_2596del (p.Asp865fs)	rs2061278560
NM_001322934.2(NFKB2):c.2600C>T (p.Ala867Val)	rs727502788

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