List of intergenic variants reported as pathogenic for orofacial cleft

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: 5

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HGVS	dbSNP	gnomAD frequency
46;X;t(X;5)(p11.23;q35)dn
46;XX;ins(5;6)(p13;p24p25)dn
46;XY;t(1;2)(p34.2;q35)dn
46;XY;t(7;8)(p12.3;p11.2)dn
NC_000001.11:g.74782030_75055193del

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