ClinVar Miner

List of variants studied for Williams syndrome by Cytogenetics and Genomics Lab, Cyprus Institute Of Neurology and Genetics

Included ClinVar conditions (2):

Cutis laxa, autosomal dominant 1; Williams syndrome; Supravalvar aortic stenosis
Williams syndrome

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_000007.14:g.73773313_74086695del

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