Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		A 0.800 CausalMutation CLINVAR Screening of AIP Gene Variations in a Cohort of Turkish Patients with Young-Onset Sporadic Hormone-Secreting Pituitary Adenomas. 30461320 2018
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		0.800 GeneticVariation UNIPROT Aryl hydrocarbon receptor interacting protein (AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas. 18410548 2008
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		0.800 GeneticVariation UNIPROT Germline mutation in the aryl hydrocarbon receptor interacting protein gene in familial somatotropinoma. 17341560 2007
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		0.800 GeneticVariation UNIPROT Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomas. 17299063 2007
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		0.800 GeneticVariation UNIPROT Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families. 17244780 2007
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		0.800 GeneticVariation UNIPROT Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations. 17360484 2007
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		0.800 GeneticVariation UNIPROT Pituitary adenoma predisposition caused by germline mutations in the AIP gene. 16728643 2006
dbSNP: rs11227805
rs11227805
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs144740330
rs144740330
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs12795957
rs12795957
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C0005890
Disease:
Body Height 		A 0.700 GeneticVariation GWASCAT Evaluation and application of summary statistic imputation to discover new height-associated loci. 29782485 2018
dbSNP: rs3741168
rs3741168
Entrez Id: 9049;80194
Gene Symbol: AIP;TMEM134
AIP;TMEM134
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs4084113
rs4084113
Entrez Id: 9049;102465450
Gene Symbol: AIP;MIR6752
AIP;MIR6752
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs104894194
rs104894194
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894194
rs104894194
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C1863340
Disease:
PITUITARY ADENOMA PREDISPOSITION (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894195
rs104894195
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121908356
rs121908356
Entrez Id: 9049;102465450
Gene Symbol: AIP;MIR6752
AIP;MIR6752
CUI: C1863340
Disease:
PITUITARY ADENOMA PREDISPOSITION (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121908357
rs121908357
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		T 0.700 CausalMutation CLINVAR
dbSNP: rs267606555
rs267606555
Entrez Id: 9049;102465450
Gene Symbol: AIP;MIR6752
AIP;MIR6752
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		A 0.700 CausalMutation CLINVAR
dbSNP: rs267606559
rs267606559
Entrez Id: 9049;102465450
Gene Symbol: AIP;MIR6752
AIP;MIR6752
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		C 0.700 CausalMutation CLINVAR
dbSNP: rs267606567
rs267606567
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		G 0.700 CausalMutation CLINVAR
dbSNP: rs267606580
rs267606580
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C4538355
Disease:
PITUITARY ADENOMA 1, MULTIPLE TYPES 		CA 0.700 CausalMutation CLINVAR
dbSNP: rs886037871
rs886037871
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C2676191
Disease:
PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder) 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1287485768
rs1287485768
Entrez Id: 9049;102465450
Gene Symbol: AIP;MIR6752
AIP;MIR6752
CUI: C2676191
Disease:
PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder) 		0.010 GeneticVariation BEFREE A novel missense mutation (c.512C>T, p.T171I) was discovered in 3 patients from a Chinese family with familial isolated pituitary adenoma. 30447469 2019
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C0032000
Disease:
Pituitary Adenoma 		0.010 GeneticVariation BEFREE The AIP c.911G>A: p.Arg304Gln (rs104894190) variant was detected in only two patients with functional PA: one with somatotropinoma [in 1/55 (1.8%)] and one with prolactinoma [in 1/25 (4%)]. 30461320 2018
dbSNP: rs104894190
rs104894190
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C0033375
Disease:
Prolactinoma 		0.010 GeneticVariation BEFREE The AIP c.911G>A: p.Arg304Gln (rs104894190) variant was detected in only two patients with functional PA: one with somatotropinoma [in 1/55 (1.8%)] and one with prolactinoma [in 1/25 (4%)]. 30461320 2018