rs1384936174, NOD2

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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.100 1.000 13 2007 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.040 0.750 4 2008 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.030 1.000 3 2007 2009
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2008 2008
Necrotizing Enterocolitis
CUI: C0520459
Disease: Necrotizing Enterocolitis
7 0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2017 2017
Necrotizing enterocolitis in fetus OR newborn
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
26 0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2017 2017