Gene: MIR4321 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs149082963
rs149082963
AMH ; MIR4321
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: rs371874189
rs371874189
AMH ; MIR4321
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: rs569914235
rs569914235
AMH ; MIR4321
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
AMH ; MIR4321
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: rs149082963
rs149082963
AMH ; MIR4321
0.700 GeneticVariation UNIPROT Molecular genetics of the persistent müllerian duct syndrome: a study of 19 families. 8162013

1994
dbSNP: rs371874189
rs371874189
AMH ; MIR4321
0.700 GeneticVariation UNIPROT Molecular genetics of the persistent müllerian duct syndrome: a study of 19 families. 8162013

1994
dbSNP: rs569914235
rs569914235
AMH ; MIR4321
0.700 GeneticVariation UNIPROT Molecular genetics of the persistent müllerian duct syndrome: a study of 19 families. 8162013

1994
dbSNP: rs777003373
rs777003373
AMH ; MIR4321
0.700 GeneticVariation UNIPROT Molecular genetics of the persistent müllerian duct syndrome: a study of 19 families. 8162013

1994
dbSNP: rs104894666
rs104894666
AMH ; MIR4321
T 0.700 CausalMutation CLINVAR