List of variants in gene LOC121815964, NFKB2 studied for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001322934.2(NFKB2):c.662-11C>T	rs4919632	0.92540
NM_001322934.2(NFKB2):c.736G>A (p.Val246Ile)	rs368808361	0.00021
NM_001322934.2(NFKB2):c.669G>A (p.Pro223=)	rs748619086	0.00004
NM_001322934.2(NFKB2):c.722G>A (p.Arg241Gln)	rs772667682	0.00002
NM_001322934.2(NFKB2):c.662-5C>T	rs1469839251	0.00001
NM_001322934.2(NFKB2):c.662-14A>C
NM_001322934.2(NFKB2):c.662-7T>G
NM_001322934.2(NFKB2):c.662A>G (p.Lys221Arg)	rs2061147566
NM_001322934.2(NFKB2):c.669G>C (p.Pro223=)
NM_001322934.2(NFKB2):c.672G>A (p.Gly224=)
NM_001322934.2(NFKB2):c.673dup (p.Ala225fs)	rs2061147687
NM_001322934.2(NFKB2):c.710C>T (p.Ala237Val)
NM_001322934.2(NFKB2):c.719_720del (p.Val240fs)
NM_001322934.2(NFKB2):c.720G>A (p.Val240=)
NM_001322934.2(NFKB2):c.729A>C (p.Gly243=)	rs2061148367
NM_001322934.2(NFKB2):c.742C>G (p.Leu248Val)	rs2061148628

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