List of variants in gene AMH reported as uncertain significance 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.802A>G (p.Thr268Ala)	rs201324658	0.00034
NM_000479.5(AMH):c.295A>T (p.Thr99Ser)	rs200226465	0.00029
NM_000479.5(AMH):c.1193C>T (p.Pro398Leu)	rs368933314
NM_000479.5(AMH):c.1211T>C (p.Leu404Pro)
NM_000479.5(AMH):c.864C>G (p.Asp288Glu)	rs199831511

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