AVP, arginine vasopressin, 551

N. diseases: 78; N. variants: 18
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121964882
rs121964882
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964883
rs121964883
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964885
rs121964885
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964886
rs121964886
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964887
rs121964887
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964888
rs121964888
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964890
rs121964890
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964891
rs121964891
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964893
rs121964893
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs28934878
rs28934878
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs387906511
rs387906511
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs387906512
rs387906512
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs74315383
rs74315383
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety. 15538939 2004
dbSNP: rs121964882
rs121964882
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus. 12931042 2003
dbSNP: rs121964882
rs121964882
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation encoding Cys73Phe in neurophysin II is associated with autosomal dominant neurohypophyseal diabetes insipidus. 12359138 2003
dbSNP: rs121964882
rs121964882
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A signal peptide mutation of the arginine vasopressin gene in monozygotic twins. 12519420 2003
dbSNP: rs121964883
rs121964883
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation encoding Cys73Phe in neurophysin II is associated with autosomal dominant neurohypophyseal diabetes insipidus. 12359138 2003
dbSNP: rs121964883
rs121964883
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus. 12931042 2003
dbSNP: rs121964883
rs121964883
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A signal peptide mutation of the arginine vasopressin gene in monozygotic twins. 12519420 2003
dbSNP: rs121964885
rs121964885
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A signal peptide mutation of the arginine vasopressin gene in monozygotic twins. 12519420 2003
dbSNP: rs121964885
rs121964885
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus. 12931042 2003
dbSNP: rs121964885
rs121964885
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation encoding Cys73Phe in neurophysin II is associated with autosomal dominant neurohypophyseal diabetes insipidus. 12359138 2003
dbSNP: rs121964886
rs121964886
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A signal peptide mutation of the arginine vasopressin gene in monozygotic twins. 12519420 2003
dbSNP: rs121964886
rs121964886
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation encoding Cys73Phe in neurophysin II is associated with autosomal dominant neurohypophyseal diabetes insipidus. 12359138 2003
dbSNP: rs121964886
rs121964886
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus. 12931042 2003