List of intergenic variants reported as pathogenic for congenital hypogonadotropic hypogonadism

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: 3

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HGVS	dbSNP	gnomAD frequency
46;X;t(X;5)(q24;q13)dn
NC_000007.14:g.62535490A>G	rs483352872
NC_000011.10:g.61969097_61969098insGA

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