ClinVar Miner

List of variants in gene IKBKG reported as uncertain significance for IKBKG-related immunodeficiency with or without ectodermal dysplasia

Included ClinVar conditions (7):

Ectodermal dysplasia and immunodeficiency 1
Immunodeficiency 33
Immunodeficiency 33; Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome; Ectodermal dysplasia and immunodeficiency 1; Incontinentia pigmenti syndrome
Immunodeficiency 33; Ectodermal dysplasia and immunodeficiency 1
Immunodeficiency 33; Ectodermal dysplasia and immunodeficiency 1; Incontinentia pigmenti syndrome
Immunodeficiency 33; Ectodermal dysplasia and immunodeficiency 1; Incontinentia pigmenti syndrome; Autoinflammatory disease, X-linked
Immunodeficiency 33; Ectodermal dysplasia and immunodeficiency 1; Incontinentia pigmenti syndrome; Immunodeficiency 47

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001099857.5(IKBKG):c.399+19G>C	rs386134239	0.00223
NM_001099857.5(IKBKG):c.518+7C>T	rs386134241	0.00200
NM_001099857.5(IKBKG):c.1056-6=	rs5945206
NM_001099857.5(IKBKG):c.399+6C>T	rs1557236080
NM_001099857.5(IKBKG):c.760C>G (p.Arg254Gly)	rs2148383298

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