Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145047094
rs145047094
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE Co-occurrence of <i>MEN1</i> p.Gly111fs and <i>AIP</i> p.Arg16His Variants in Familial MEN1 Phenotype. 29848728 2018
dbSNP: rs4930199
rs4930199
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE These results suggest that Q228K and Q307R variants in the AIP gene might be involved in the genetic susceptibility to familial and sporadic pituitary adenomas (somatotrophinoma and corticotrophinoma) in the Turkish population. 25938168 2015
dbSNP: rs641081
rs641081
Entrez Id: 9049;102465450
Gene Symbol: AIP;MIR6752
AIP;MIR6752
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE These results suggest that Q228K and Q307R variants in the AIP gene might be involved in the genetic susceptibility to familial and sporadic pituitary adenomas (somatotrophinoma and corticotrophinoma) in the Turkish population. 25938168 2015