FKBP5, FKBP prolyl isomerase 5, 2289

N. diseases: 179; N. variants: 20
Disease: Rumination Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1360780
rs1360780
Entrez Id: 2289;112267956
Gene Symbol: FKBP5;LOC112267956
FKBP5;LOC112267956
CUI: C0154575
Disease:
Rumination Disorders 		0.010 GeneticVariation BEFREE We hypothesized that adolescent carriers of the FKBP5 CATT haplotype composed of rs9296158, rs3800373, rs1360780, and rs9470080, that has been associated with increased risk for psychiatric disorders in adulthood, would also show higher levels of rumination and catastrophizing. 28654774 2017
dbSNP: rs9470080
rs9470080
Entrez Id: 2289
Gene Symbol: FKBP5
FKBP5
CUI: C0154575
Disease:
Rumination Disorders 		0.010 GeneticVariation BEFREE We hypothesized that adolescent carriers of the FKBP5 CATT haplotype composed of rs9296158, rs3800373, rs1360780, and rs9470080, that has been associated with increased risk for psychiatric disorders in adulthood, would also show higher levels of rumination and catastrophizing. 28654774 2017