ClinVar Miner

List of variants studied for chromosome 22q11.2 deletion syndrome, distal by Centogene AG - the Rare Disease Company

Included ClinVar conditions (1):

Chromosome 22q11.2 deletion syndrome, distal

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000022.10:g.21514655_22986816del

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