ClinVar Miner

List of variants reported as uncertain significance for T-B+ severe combined immunodeficiency by OMIM

Included ClinVar conditions (13):

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_002185.5(IL7R):c.412G>A (p.Val138Ile)	rs1494555	0.72524
NM_002185.5(IL7R):c.197T>C (p.Ile66Thr)	rs1494558	0.68368

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