rs1414334, HTR2C

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.851 0.160 X 114903581 intron variant C/G snv 0.050 0.800 5 2007 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.851 0.160 X 114903581 intron variant C/G snv 0.020 2 2014 2015
Autistic behavior
CUI: C0856975
Disease: Autistic behavior
78 0.851 0.160 X 114903581 intron variant C/G snv 0.010 1.000 1 2010 2010
Obesity
CUI: C0028754
Disease: Obesity
1111 0.851 0.160 X 114903581 intron variant C/G snv 0.010 1.000 1 2007 2007
Pervasive Development Disorder
CUI: C0524528
Disease: Pervasive Development Disorder
49 0.851 0.160 X 114903581 intron variant C/G snv 0.010 1.000 1 2010 2010