rs41279104, NOS1

N. diseases: 6
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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.030 1.000 3 2011 2019
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.010 1.000 1 2014 2014
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.010 1.000 1 2011 2011
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.010 1 2010 2010
Pyloric Stenosis, Hypertrophic
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
306 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.010 1.000 1 2009 2009
Pyloric Stenosis, Infantile Hypertrophic 1
3 0.827 0.160 12 117439680 intron variant C/T snv 0.11 0.010 1.000 1 2009 2009