rs10758669, None

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 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.850 1.000 8 2008 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.830 1.000 6 2010 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.810 1.000 2 2012 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
Acute anterior uveitis
CUI: C0701807
Disease: Acute anterior uveitis
30 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.010 1.000 1 2016 2016
Perianal Crohn's disease
CUI: C0341395
Disease: Perianal Crohn's disease
3 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.010 1.000 1 2016 2016