rs2903692, CLEC16A

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.
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.840 1.000 4 2007 2010
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.010 1.000 1 2009 2009
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.010 1.000 1 2009 2009
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.010 1.000 1 2009 2009
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.010 1.000 1 2009 2009
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.010 1.000 1 2010 2010