Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1358787117
rs1358787117
Entrez Id: 268
Gene Symbol: AMH
AMH
CUI: C1849930
Disease:
Persistent Mullerian duct syndrome
0.700 GeneticVariation UNIPROT A 27 base-pair deletion of the anti-müllerian type II receptor gene is the most common cause of the persistent müllerian duct syndrome. 8872466 1996
dbSNP: rs1358787117
rs1358787117
Entrez Id: 268
Gene Symbol: AMH
AMH
CUI: C1849930
Disease:
Persistent Mullerian duct syndrome
0.700 GeneticVariation UNIPROT Molecular genetics of the persistent müllerian duct syndrome: a study of 19 families. 8162013 1994