List of variants in gene MCM9 reported as likely pathogenic for 46,XX ovarian dysgenesis-short stature syndrome

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_017696.3(MCM9):c.1151-1G>A
NM_017696.3(MCM9):c.139_140del (p.Leu47fs)
NM_017696.3(MCM9):c.1529-7C>G
NM_017696.3(MCM9):c.1556G>A (p.Trp519Ter)

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