Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs777003373
rs777003373
Entrez Id: 268;100423031
Gene Symbol: AMH;MIR4321
AMH;MIR4321
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: rs777003373
rs777003373
Entrez Id: 268;100423031
Gene Symbol: AMH;MIR4321
AMH;MIR4321
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