ClinVar Miner

List of intergenic variants reported as pathogenic for isolated congenital growth hormone deficiency

Included ClinVar conditions (10):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000007.14:g.62535490A>G	rs483352872

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