List of variants in gene NFKB2 reported as benign for hematologic disorder

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001322934.2(NFKB2):c.1821A>G (p.Ala607=)	rs4919634	0.99720
NM_001322934.2(NFKB2):c.2467-9T>A	rs11574853	0.05268
NM_001322934.2(NFKB2):c.2094C>T (p.Asn698=)	rs11574851	0.03687
NM_001322934.2(NFKB2):c.2239C>T (p.Leu747=)	rs11191279	0.01026
NM_001322934.2(NFKB2):c.1869G>A (p.Gly623=)	rs138786808	0.00361
NM_001322934.2(NFKB2):c.21+13G>A	rs199513883	0.00288
NM_001322934.2(NFKB2):c.1821= (p.Ala607=)	rs4919634	0.00280
NM_001322934.2(NFKB2):c.1962C>T (p.Val654=)	rs201623844	0.00221
NM_001322934.2(NFKB2):c.1826G>A (p.Arg609Gln)	rs200092317	0.00151
NM_001322934.2(NFKB2):c.2145G>A (p.Ser715=)	rs200006038	0.00128
NM_001322934.2(NFKB2):c.2224-15C>T	rs142623210	0.00125
NM_001322934.2(NFKB2):c.1608C>A (p.Ile536=)	rs34916280	0.00083
NM_001322934.2(NFKB2):c.921G>A (p.Leu307=)	rs146926941	0.00064
NM_001322934.2(NFKB2):c.2224-10G>A	rs550812736	0.00034
NM_001322934.2(NFKB2):c.1117+7G>T	rs188346889	0.00026
NM_001322934.2(NFKB2):c.1953C>G (p.Thr651=)	rs372873787	0.00022
NM_001322934.2(NFKB2):c.978C>T (p.Tyr326=)	rs2295587	0.00016
NM_001322934.2(NFKB2):c.243+20G>C	rs371813362	0.00014
NM_001322934.2(NFKB2):c.1539C>T (p.His513=)	rs533142885	0.00010
NM_001322934.2(NFKB2):c.503-16T>C	rs201456641	0.00009
NM_001322934.2(NFKB2):c.2475C>T (p.Gly825=)	rs200482499	0.00008
NM_001322934.2(NFKB2):c.1969-17G>A	rs375150780	0.00006
NM_001322934.2(NFKB2):c.503-17A>G	rs201960564	0.00006
NM_001322934.2(NFKB2):c.767-13G>A	rs746075690	0.00004
NM_001322934.2(NFKB2):c.853-8C>A	rs749266689	0.00003
NM_001322934.2(NFKB2):c.1584+11G>A
NM_001322934.2(NFKB2):c.1584+9dup	rs935753166
NM_001322934.2(NFKB2):c.1821A>C (p.Ala607=)
NM_001322934.2(NFKB2):c.502+16dup
NM_001322934.2(NFKB2):c.502+22_502+45del

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