List of intergenic variants reported as uncertain significance for corneal disorder

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: 6

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HGVS	dbSNP	gnomAD frequency
46;XX;t(X;22)(q13;q13)
46;XY;t(18;20)(q21.1;p11.23)dn
46;XY;t(6;20)(p12;q13.1)dn
NC_000004.12:g.69391612A>G
NC_000007.14:g.129126742_129126748del
NT_113889.1:g.54175G>A

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