Submissions for variant NM_020529.3(NFKBIA):c.548-3C>T

gnomAD frequency: 0.00648  dbSNP: rs2233418

Total submissions: 5

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Illumina Laboratory Services, Illumina	RCV000326008	SCV000386627	benign	Ectodermal dysplasia and immunodeficiency 2	2018-01-13	criteria provided, single submitter	clinical testing	This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Labcorp Genetics (formerly Invitae), Labcorp	RCV000326008	SCV000647016	benign	Ectodermal dysplasia and immunodeficiency 2	2024-01-31	criteria provided, single submitter	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV000326008	SCV000744033	likely benign	Ectodermal dysplasia and immunodeficiency 2	2015-07-30	criteria provided, single submitter	clinical testing
CeGaT Center for Human Genetics Tuebingen	RCV002262981	SCV002545172	benign	not provided	2023-09-01	criteria provided, single submitter	clinical testing	NFKBIA: BP4, BS1, BS2
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000326008	SCV000733378	likely benign	Ectodermal dysplasia and immunodeficiency 2		no assertion criteria provided	clinical testing