rs2075820, NOD1

N. diseases: 10
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.020 0.500 2 2003 2007
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.020 0.500 2 2010 2011
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.020 1.000 2 2006 2007
Asthma
CUI: C0004096
Disease: Asthma
1536 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1.000 1 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1 2009 2009
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1.000 1 2019 2019
Guillain-Barre Syndrome
CUI: C0018378
Disease: Guillain-Barre Syndrome
13 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1.000 1 2016 2016
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1.000 1 2010 2010
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1.000 1 2010 2010
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 0.010 1.000 1 2007 2007