ClinVar Miner

List of variants reported as uncertain significance for T-cell immunodeficiency by New York Genome 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001379200.1(TBX1):c.1149_1150insAGGGCCGGC (p.Pro383_Gly384insArgAlaGly)	rs1192078635
NM_001379200.1(TBX1):c.1459A>T (p.Met487Leu)	rs1936874664

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