List of variants in gene combination LOC130055497, NFKBIA reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_020529.3(NFKBIA):c.-66G>A	rs2273651	0.00614
NM_020529.3(NFKBIA):c.-41G>A	rs540282095	0.00067

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