List of intergenic variants reported as uncertain significance for obesity 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: 5

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HGVS	dbSNP	gnomAD frequency
46;X;inv(X)(q26q28)dn
46;X;t(X;21)(q26.1;q21.22)dn
46;XX;t(7;12)(q11.2;q12).ish
46;XX;t(9;19)(q22.3;q13.1)dn
46;Y;inv(X)(q27q28)

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