List of variants in gene combination LOC130004598, NFKB2 reported as likely benign for hematologic disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001322934.2(NFKB2):c.66C>T (p.Ser22=)	rs750859613	0.00004
NM_001322934.2(NFKB2):c.22-15C>G	rs772741852	0.00002
NM_001322934.2(NFKB2):c.45T>C (p.Tyr15=)	rs764595866	0.00001
NM_001322934.2(NFKB2):c.22-18A>T
NM_001322934.2(NFKB2):c.22-7A>G	rs1175931759
NM_001322934.2(NFKB2):c.27G>A (p.Leu9=)
NM_001322934.2(NFKB2):c.51T>C (p.Asp17=)	rs762442104

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