AVP, arginine vasopressin, 551

N. diseases: 454; N. variants: 27
Source: ALL
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 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121964883
rs121964883
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121964885
rs121964885
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121964886
rs121964886
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121964887
rs121964887
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121964888
rs121964888
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		G 0.800 CausalMutation CLINVAR
dbSNP: rs121964890
rs121964890
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121964891
rs121964891
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121964893
rs121964893
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		G 0.800 CausalMutation CLINVAR
dbSNP: rs28934878
rs28934878
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		G 0.800 CausalMutation CLINVAR
dbSNP: rs387906511
rs387906511
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		T 0.800 CausalMutation CLINVAR
dbSNP: rs387906512
rs387906512
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.800 CausalMutation CLINVAR
dbSNP: rs74315383
rs74315383
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		C 0.800 CausalMutation CLINVAR
dbSNP: rs1057516192
rs1057516192
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs121964884
rs121964884
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121964889
rs121964889
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121964892
rs121964892
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C4016430
Disease:
DIABETES INSIPIDUS, NEUROHYPOPHYSEAL, AUTOSOMAL RECESSIVE 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121964882
rs121964882
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964883
rs121964883
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964885
rs121964885
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964886
rs121964886
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964887
rs121964887
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964888
rs121964888
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964890
rs121964890
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992
dbSNP: rs121964891
rs121964891
Entrez Id: 551
Gene Symbol: AVP
AVP
CUI: C0687720
Disease:
Central Diabetes Insipidus 		0.800 GeneticVariation UNIPROT A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. 1740104 1992