rs11179027, TPH2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Anorexia Nervosa
CUI: C0003125
Disease: Anorexia Nervosa
0.010 GeneticVariation BEFREE In addition, rs3825885 (NTRK3, p = 9 × 10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p = 2 × 10(-3)) as an OCD marker. 23337130 2013