FAAH2, fatty acid amide hydrolase 2, 158584

N. diseases: 11; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs139470886
rs139470886 		1.000 0.080 X 57282697 upstream gene variant G/A snv 4.3E-02
CUI: C0002170
Disease: Alopecia
Alopecia 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs144226500
rs144226500 		1.000 0.080 X 57144348 intergenic variant -/T;TT delins
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs5914101
rs5914101 		X 57413512 intron variant G/A snv 0.33
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2016 2016
dbSNP: rs7058676
rs7058676 		X 57322090 intron variant C/T snv 0.36
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019