rs11465996, LY96

N. diseases: 7
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 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.020 1.000 2 2014 2014
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.020 1.000 2 2014 2014
Carcinoma, Neuroendocrine
CUI: C0206695
Disease: Carcinoma, Neuroendocrine
7 0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.010 1.000 1 2015 2015
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.010 1.000 1 2012 2012
Necrotizing enterocolitis in fetus OR newborn
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
26 0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.010 1.000 1 2015 2015
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.010 1.000 1 2012 2012
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 0.010 1.000 1 2012 2012