AMH, anti-Mullerian hormone, 268

N. diseases: 242; N. variants: 12
Disease: Persistent Mullerian duct syndrome ×
Source: ALL
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: rs149082963
rs149082963
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: rs371874189
rs371874189
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: rs569914235
rs569914235
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 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
dbSNP: rs149082963
rs149082963
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
dbSNP: rs371874189
rs371874189
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
dbSNP: rs569914235
rs569914235
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
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
dbSNP: rs104894666
rs104894666
Entrez Id: 268;100423031
Gene Symbol: AMH;MIR4321
AMH;MIR4321
CUI: C1849930
Disease:
Persistent Mullerian duct syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs138571039
rs138571039
Entrez Id: 268;126306
Gene Symbol: AMH;JSRP1
AMH;JSRP1
CUI: C1849930
Disease:
Persistent Mullerian duct syndrome 		0.700 GeneticVariation UNIPROT
dbSNP: rs267606654
rs267606654
Entrez Id: 268
Gene Symbol: AMH
AMH
CUI: C1849930
Disease:
Persistent Mullerian duct syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs397518444
rs397518444
Entrez Id: 268
Gene Symbol: AMH
AMH
CUI: C1849930
Disease:
Persistent Mullerian duct syndrome 		GAGCTCAGCGTAGACCTCCGCGCC 0.700 CausalMutation CLINVAR