List of variants in gene AMH reported as pathogenic for Persistent Mullerian duct 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000479.5(AMH):c.151del (p.Gln51fs)	rs1443929462	0.00001
NM_000479.5(AMH):c.649C>T (p.Gln217Ter)	rs1183532981	0.00001
NM_000479.5(AMH):c.1165G>T (p.Glu389Ter)
NM_000479.5(AMH):c.209del (p.Leu70fs)
NM_000479.5(AMH):c.343_344del (p.Leu115fs)

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