List of variants in gene combination LOC130004598, NFKB2 reported as uncertain significance for immune system disorder

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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.62A>G (p.Asn21Ser)	rs577190240	0.00002
NM_001322934.2(NFKB2):c.22G>C (p.Gly8Arg)	rs922475027	0.00001
NM_001322934.2(NFKB2):c.28G>A (p.Asp10Asn)
NM_001322934.2(NFKB2):c.29A>G (p.Asp10Gly)
NM_001322934.2(NFKB2):c.48T>G (p.Asp16Glu)

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