List of variants in gene combination IKBKB, LOC126860373 reported as likely 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001556.3(IKBKB):c.388+9C>T	rs140937081	0.00022
NM_001556.3(IKBKB):c.319-10T>C	rs199743559	0.00006
NM_001556.3(IKBKB):c.349C>T (p.Leu117=)	rs202223251	0.00002
NM_001556.3(IKBKB):c.388+15C>T	rs747780454	0.00002
NM_001556.3(IKBKB):c.319-20G>C
NM_001556.3(IKBKB):c.319-5G>C
NM_001556.3(IKBKB):c.319-6T>C
NM_001556.3(IKBKB):c.384C>T (p.Asp128=)
NM_001556.3(IKBKB):c.388+10A>C
NM_001556.3(IKBKB):c.388+13C>G
NM_001556.3(IKBKB):c.388+16G>A
NM_001556.3(IKBKB):c.388+18A>C

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