List of variants in gene AMH reported as pathogenic for indeterminate sex and/or pseudohermaphroditism

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: 8

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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.1144G>T (p.Glu382Ter)	rs267606654
NM_000479.5(AMH):c.1165G>T (p.Glu389Ter)
NM_000479.5(AMH):c.1397_1419dup (p.Glu474delinsSerSerAlaTer)	rs397518444
NM_000479.5(AMH):c.209del (p.Leu70fs)
NM_000479.5(AMH):c.343_344del (p.Leu115fs)
NM_000479.5(AMH):c.472_485del (p.Pro158fs)	rs774592796

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