"PreventionGenetics, part of Exact Sciences"[submitter] AND "AMH"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 381731	NM_000479.5(AMH):c.35T>G (p.Val12Gly)	AMH, LOC108783649 (V12G)	Single nucleotide variant (missense variant)	AMH-related disorder +1 more	GUncertain significance
Select item 745907	NM_000479.5(AMH):c.273C>T (p.Arg91=)	AMH	Single nucleotide variant (synonymous variant)	AMH-related disorder +1 more	GLikely benign
Select item 2066260	NM_000479.5(AMH):c.304G>A (p.Val102Ile)	AMH (V102I)	Single nucleotide variant (missense variant)	AMH-related disorder +1 more	GBenign
Select item 3035111	NM_000479.5(AMH):c.849G>A (p.Ser283=)	AMH	Single nucleotide variant (synonymous variant)	AMH-related disorder	GLikely benign
Select item 1435809	NM_000479.5(AMH):c.905G>A (p.Arg302Gln)	AMH (R302Q)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1591512	NM_000479.5(AMH):c.950C>G (p.Pro317Arg)	AMH (P317R)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 752683	NM_000479.5(AMH):c.1620G>A (p.Ser540=)	AMH	Single nucleotide variant (synonymous variant)	AMH-related disorder +1 more	GLikely benign

ClinVar