List of variants in gene NFKB1 reported as likely pathogenic by NIHR Bioresource Rare Diseases, University of Cambridge

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003998.4(NFKB1):c.160-1G>A	rs1578735709
NM_003998.4(NFKB1):c.187del (p.Glu63fs)	rs1578735747
NM_003998.4(NFKB1):c.835+2T>C	rs869320689
NM_003998.4(NFKB1):c.850C>T (p.Arg284Ter)	rs1578793312
NM_003998.4(NFKB1):c.904dup (p.Ser302fs)	rs773694113

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