{{Rsnum
|rsid=10407022
|Gene=AMH
|Chromosome=19
|position=2249478
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.3269
|Gene_s=AMH,MIR4321
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 2.7 | 30.1 | 67.3
| HCB | 17.9 | 49.3 | 32.8
| JPT | 5.6 | 50.0 | 44.4
| YRI | 19.7 | 50.8 | 29.5
| ASW | 12.5 | 44.6 | 42.9
| CHB | 17.9 | 49.3 | 32.8
| CHD | 14.4 | 52.9 | 32.7
| GIH | 5.0 | 29.7 | 65.3
| LWK | 30.0 | 50.9 | 19.1
| MEX | 12.5 | 39.3 | 48.2
| MKK | 25.8 | 49.7 | 24.5
| TSI | 2.0 | 32.7 | 65.3
| HapMapRevision=28
}}{{Venter SNP
|rsid=10407022
|allele=T
|frequency=0.805
|uid=1103691072201
|type=homozygous_SNP
|hugo=AMH
|ensembl gene=ENSG00000104899
|ensembl transcript=ENST00000221496
|sift=AFFECT FUNCTION
|disease=Defects in AMH are the cause of persistent Muellerian duct syndrome type I (PMDS-1) (MIM:261550). PMDS-1 is a form of male pseudohermaphroditism characterized by a failure of Muellerian duct regression in otherwise normal males.
}}

{{PMID Auto
|PMID=17636279
|Title=A polymorphism in the AMH type II receptor gene is associated with age at menopause in interaction with parity.
}}

{{PMID Auto
|PMID=18230658
|Title=A functional anti-mullerian hormone gene polymorphism is associated with follicle number and androgen levels in polycystic ovary syndrome patients.
}}

{{PMID Auto
|PMID=18603647
|Title=Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
|OA=1
}}

{{GET Evidence
|gene=AMH
|aa_change=Ser49Ile
|aa_change_short=S49I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10407022
|overall_frequency_n=7910
|overall_frequency_d=10728
|overall_frequency=0.737323
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=81
|n_articles=0
|n_articles_annotated=0
|nblosum100=5
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23544102
|Title=Interactions between genetic variants in AMH and AMHR2 may modify age at natural menopause
|OA=1
}}

{{PMID Auto
|PMID=23371438
|Title=Haplotype analysis of single nucleotide polymorphisms in anti-Mullerian hormone gene in Chinese PCOS women.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}