ClinVar Miner

List of variants reported as likely pathogenic for chromosome 22q deletion by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (8):

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
NC_000022.10:g.(?_19748408)_(19748823_?)dup
NM_001379200.1(TBX1):c.711+1G>A	rs1731409120
NM_080647.1(TBX1):c.34+2T>A

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