List of variants in gene NFKB2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_001322934.2(NFKB2):c.1826G>A (p.Arg609Gln)	rs200092317	0.00151
NM_001322934.2(NFKB2):c.1736G>A (p.Arg579His)	rs200227171	0.00065
NM_001077494.3(NFKB2):c.-72-473G>A
NM_001322934.2(NFKB2):c.502+22_502+45del
NM_002502.5(NFKB2):c.-232C>A

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