List of variants in gene HROB reported as pathogenic for Ovarian dysgenesis 11

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
NM_001171251.3(HROB):c.421del (p.Glu141fs)	rs762836620	0.00001
NM_001171251.3(HROB):c.1351C>T (p.Arg451Ter)
NM_001171251.3(HROB):c.718C>T (p.Arg240Ter)

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