rs3763313, BTNL2

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.
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2013 2013
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.010 1.000 1 2015 2015
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2008 2008
Diabetes Mellitus, Insulin-Dependent
954 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2007 2007
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2013 2013
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2012 2012
Oral Ulcer
CUI: C0149745
Disease: Oral Ulcer
101 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2019 2019