ClinVar Miner

List of variants reported as pathogenic for T-cell immunodeficiency by Institute of Human Genetics, University of Leipzig Medical Center

Included ClinVar conditions (5):

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: 3

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 22p13(chr22:135350-150557)x1
GRCh37/hg19 22q11.21(chr22:18893838-20307561)x1
NM_001379200.1(TBX1):c.711+1G>A	rs1731409120

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