ClinVar Miner

List of variants reported as likely benign for severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency by Genome Diagnostics Laboratory, University Medical Center Utrecht

Included ClinVar conditions (2):

Partial adenosine deaminase deficiency
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_000022.4(ADA):c.162G>A (p.Lys54=)	rs45557242	0.00282
NM_000022.4(ADA):c.606+10G>A	rs201045221	0.00058

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