ClinVar Miner

List of variants reported as pathogenic for T-B+ severe combined immunodeficiency due to gamma chain deficiency by Klein lab, Ludwig-Maximilians-University

Included ClinVar conditions (2):

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_000206.3(IL2RG):c.87del (p.Asn31fs)	rs1602289943

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